Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))

Wojciech Wiszniewski; Jill V. Hunter; Neil A. Hanchard; Jason R. Willer; Chad Shaw; Qi Tian; Anna Illner; Xueqing Wang; Sau W. Cheung; Ankita Patel; Ian M. Campbell; Violet Gelowani; Patricia Hixson; Audrey R. Ester; Mahshid S. Azamian; Lorraine Potocki; Gladys Zapata; Patricia P. Hernandez; Melissa B. Ramocki; Regie L.P. Santos-Cortez; Gao Wang; Michele K. York; Monica J. Justice; Zili D. Chu; Patricia I. Bader; Lisa Omo-Griffith; Nirupama S. Madduri; Gunter Scharer; Heather P. Crawford; Pattamawadee Yanatatsaneejit; Anna Eifert; Jeffery Kerr; Carlos A. Bacino; Adiaha I.A. Franklin; Robin Goin-Kochel; Gayle Simpson; Ladonna Immken; Muhammad E. Haque; Marija Stosic; Misti D. Williams; Thomas M. Morgan; Sumit Pruthi; Reed Omary; Simeon A. Boyadjiev; Kay K. Win; Aye Thida; Matthew Hurles; Martin Lloyd Hibberd; Chiea Chuen Khor; Nguyen Van Vinh Chau; Thomas E. Gallagher; Apiwat Mutirangura; Pawel Stankiewicz; Arthur L. Beaudet; Mirjana Maletic-Savatic; Jill A. Rosenfeld; Lisa G. Shaffer; Erica E. Davis; John W. Belmont; Sarah Dunstan; Cameron P. Simmons; Penelope E. Bonnen; Suzanne M. Leal; Nicholas Katsanis; James R. Lupski; Seema R. Lalani

doi:10.1016/j.ajhg.2013.07.001

Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))

Wojciech Wiszniewski, Jill V. Hunter, Neil A. Hanchard, Jason R. Willer, Chad Shaw, Qi Tian, Anna Illner, Xueqing Wang, Sau W. Cheung, Ankita Patel, Ian M. Campbell, Violet Gelowani, Patricia Hixson, Audrey R. Ester, Mahshid S. Azamian, Lorraine Potocki, Gladys Zapata, Patricia P. Hernandez, Melissa B. Ramocki, Regie L.P. Santos-CortezGao Wang, Michele K. York, Monica J. Justice, Zili D. Chu, Patricia I. Bader, Lisa Omo-Griffith, Nirupama S. Madduri, Gunter Scharer, Heather P. Crawford, Pattamawadee Yanatatsaneejit, Anna Eifert, Jeffery Kerr, Carlos A. Bacino, Adiaha I.A. Franklin, Robin Goin-Kochel, Gayle Simpson, Ladonna Immken, Muhammad E. Haque, Marija Stosic, Misti D. Williams, Thomas M. Morgan, Sumit Pruthi, Reed Omary, Simeon A. Boyadjiev, Kay K. Win, Aye Thida, Matthew Hurles, Martin Lloyd Hibberd, Chiea Chuen Khor, Nguyen Van Vinh Chau, Thomas E. Gallagher, Apiwat Mutirangura, Pawel Stankiewicz, Arthur L. Beaudet, Mirjana Maletic-Savatic, Jill A. Rosenfeld, Lisa G. Shaffer, Erica E. Davis, John W. Belmont, Sarah Dunstan, Cameron P. Simmons, Penelope E. Bonnen, Suzanne M. Leal, Nicholas Katsanis, James R. Lupski, Seema R. Lalani^*

^*Corresponding author for this work

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

(The American Journal of Human Genetics 93, 197–210; August 8, 2013) In the version published online on June 27, 2013, the affiliations included a few errors. In addition, the author Violet Gelowani was accidently omitted from the author list. All of these mistakes have been corrected in the online and the print versions of the article and appear correctly here. The authors and The Journal regret the errors.

Original language	English (US)
Pages (from-to)	405
Number of pages	1
Journal	American journal of human genetics
Volume	93
Issue number	2
DOIs	https://doi.org/10.1016/j.ajhg.2013.07.001
State	Published - Aug 8 2013
Externally published	Yes

Funding

We are indebted to the families who participated in this research study. Support for this work was provided by the Doris Duke Charitable Foundation (DDCF) and Gillson Longenbaugh Foundation to S.R.L., National Institutes of Health (RO1-HL091771) to J.W.B. and S.R.L., NINDS (RO1-NS058529-03) and NHGRI (5U54HG006542) to J.R.L.; and NIMH (P50-MH094268) and a grant from the Simons Foundation (SFARI # 239983) to N.K. W.W. is supported by a Career Development Award K23NS078056 grant from the NINDS and Molecular Medicine Scholars Program at BCM (HL-66991). M.B.R. is grateful for the support of grant 5K08NS062711 from the NIH/NINDS. M.M.-S. was supported by the McKnight Endowment for Science, Dana Foundation, and the NIH Intellectual and the Developmental Disabilities Research Grant (P30HD024064). S.A.B. is partially funded by a Children’s Miracle Network endowed chair in pediatric genetics. N.K. is a Distinguished Jean and George W. Brumley Professor. We thank Emily Hall and Jillian Pearring for technical support. The Department of Molecular and Human Genetics at Baylor College of Medicine offers extensive genetic laboratory testing, including chromosomal microarray analysis, and derives revenue from this activity. J.A.R. is an employee of Signature Genomic Laboratories, a subsidiary of PerkinElmer, Inc.

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Wiszniewski, W., Hunter, J. V., Hanchard, N. A., Willer, J. R., Shaw, C., Tian, Q., Illner, A., Wang, X., Cheung, S. W., Patel, A., Campbell, I. M., Gelowani, V., Hixson, P., Ester, A. R., Azamian, M. S., Potocki, L., Zapata, G., Hernandez, P. P., Ramocki, M. B., ... Lalani, S. R. (2013). Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027)). American journal of human genetics, 93(2), 405. https://doi.org/10.1016/j.ajhg.2013.07.001

Wiszniewski, Wojciech ; Hunter, Jill V. ; Hanchard, Neil A. et al. / Erratum : TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027)). In: American journal of human genetics. 2013 ; Vol. 93, No. 2. pp. 405.

@article{f572380951194b99aa5d1a17e344c112,

title = "Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))",

abstract = "(The American Journal of Human Genetics 93, 197–210; August 8, 2013) In the version published online on June 27, 2013, the affiliations included a few errors. In addition, the author Violet Gelowani was accidently omitted from the author list. All of these mistakes have been corrected in the online and the print versions of the article and appear correctly here. The authors and The Journal regret the errors.",

author = "Wojciech Wiszniewski and Hunter, {Jill V.} and Hanchard, {Neil A.} and Willer, {Jason R.} and Chad Shaw and Qi Tian and Anna Illner and Xueqing Wang and Cheung, {Sau W.} and Ankita Patel and Campbell, {Ian M.} and Violet Gelowani and Patricia Hixson and Ester, {Audrey R.} and Azamian, {Mahshid S.} and Lorraine Potocki and Gladys Zapata and Hernandez, {Patricia P.} and Ramocki, {Melissa B.} and Santos-Cortez, {Regie L.P.} and Gao Wang and York, {Michele K.} and Justice, {Monica J.} and Chu, {Zili D.} and Bader, {Patricia I.} and Lisa Omo-Griffith and Madduri, {Nirupama S.} and Gunter Scharer and Crawford, {Heather P.} and Pattamawadee Yanatatsaneejit and Anna Eifert and Jeffery Kerr and Bacino, {Carlos A.} and Franklin, {Adiaha I.A.} and Robin Goin-Kochel and Gayle Simpson and Ladonna Immken and Haque, {Muhammad E.} and Marija Stosic and Williams, {Misti D.} and Morgan, {Thomas M.} and Sumit Pruthi and Reed Omary and Boyadjiev, {Simeon A.} and Win, {Kay K.} and Aye Thida and Matthew Hurles and Hibberd, {Martin Lloyd} and Khor, {Chiea Chuen} and {Van Vinh Chau}, Nguyen and Gallagher, {Thomas E.} and Apiwat Mutirangura and Pawel Stankiewicz and Beaudet, {Arthur L.} and Mirjana Maletic-Savatic and Rosenfeld, {Jill A.} and Shaffer, {Lisa G.} and Davis, {Erica E.} and Belmont, {John W.} and Sarah Dunstan and Simmons, {Cameron P.} and Bonnen, {Penelope E.} and Leal, {Suzanne M.} and Nicholas Katsanis and Lupski, {James R.} and Lalani, {Seema R.}",

note = "Publisher Copyright: {\textcopyright} 2013 The American Society of Human Genetics",

year = "2013",

month = aug,

day = "8",

doi = "10.1016/j.ajhg.2013.07.001",

language = "English (US)",

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journal = "American journal of human genetics",

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Wiszniewski, W, Hunter, JV, Hanchard, NA, Willer, JR, Shaw, C, Tian, Q, Illner, A, Wang, X, Cheung, SW, Patel, A, Campbell, IM, Gelowani, V, Hixson, P, Ester, AR, Azamian, MS, Potocki, L, Zapata, G, Hernandez, PP, Ramocki, MB, Santos-Cortez, RLP, Wang, G, York, MK, Justice, MJ, Chu, ZD, Bader, PI, Omo-Griffith, L, Madduri, NS, Scharer, G, Crawford, HP, Yanatatsaneejit, P, Eifert, A, Kerr, J, Bacino, CA, Franklin, AIA, Goin-Kochel, R, Simpson, G, Immken, L, Haque, ME, Stosic, M, Williams, MD, Morgan, TM, Pruthi, S, Omary, R, Boyadjiev, SA, Win, KK, Thida, A, Hurles, M, Hibberd, ML, Khor, CC, Van Vinh Chau, N, Gallagher, TE, Mutirangura, A, Stankiewicz, P, Beaudet, AL, Maletic-Savatic, M, Rosenfeld, JA, Shaffer, LG, Davis, EE, Belmont, JW, Dunstan, S, Simmons, CP, Bonnen, PE, Leal, SM, Katsanis, N, Lupski, JR & Lalani, SR 2013, 'Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))', American journal of human genetics, vol. 93, no. 2, pp. 405. https://doi.org/10.1016/j.ajhg.2013.07.001

Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027)). / Wiszniewski, Wojciech; Hunter, Jill V.; Hanchard, Neil A. et al.
In: American journal of human genetics, Vol. 93, No. 2, 08.08.2013, p. 405.

Research output: Contribution to journal › Comment/debate › peer-review

TY - JOUR

T1 - Erratum

T2 - TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))

AU - Wiszniewski, Wojciech

AU - Hunter, Jill V.

AU - Hanchard, Neil A.

AU - Willer, Jason R.

AU - Shaw, Chad

AU - Tian, Qi

AU - Illner, Anna

AU - Wang, Xueqing

AU - Cheung, Sau W.

AU - Patel, Ankita

AU - Campbell, Ian M.

AU - Gelowani, Violet

AU - Hixson, Patricia

AU - Ester, Audrey R.

AU - Azamian, Mahshid S.

AU - Potocki, Lorraine

AU - Zapata, Gladys

AU - Hernandez, Patricia P.

AU - Ramocki, Melissa B.

AU - Santos-Cortez, Regie L.P.

AU - Wang, Gao

AU - York, Michele K.

AU - Justice, Monica J.

AU - Chu, Zili D.

AU - Bader, Patricia I.

AU - Omo-Griffith, Lisa

AU - Madduri, Nirupama S.

AU - Scharer, Gunter

AU - Crawford, Heather P.

AU - Yanatatsaneejit, Pattamawadee

AU - Eifert, Anna

AU - Kerr, Jeffery

AU - Bacino, Carlos A.

AU - Franklin, Adiaha I.A.

AU - Goin-Kochel, Robin

AU - Simpson, Gayle

AU - Immken, Ladonna

AU - Haque, Muhammad E.

AU - Stosic, Marija

AU - Williams, Misti D.

AU - Morgan, Thomas M.

AU - Pruthi, Sumit

AU - Omary, Reed

AU - Boyadjiev, Simeon A.

AU - Win, Kay K.

AU - Thida, Aye

AU - Hurles, Matthew

AU - Hibberd, Martin Lloyd

AU - Khor, Chiea Chuen

AU - Van Vinh Chau, Nguyen

AU - Gallagher, Thomas E.

AU - Mutirangura, Apiwat

AU - Stankiewicz, Pawel

AU - Beaudet, Arthur L.

AU - Maletic-Savatic, Mirjana

AU - Rosenfeld, Jill A.

AU - Shaffer, Lisa G.

AU - Davis, Erica E.

AU - Belmont, John W.

AU - Dunstan, Sarah

AU - Simmons, Cameron P.

AU - Bonnen, Penelope E.

AU - Leal, Suzanne M.

AU - Katsanis, Nicholas

AU - Lupski, James R.

AU - Lalani, Seema R.

PY - 2013/8/8

Y1 - 2013/8/8

N2 - (The American Journal of Human Genetics 93, 197–210; August 8, 2013) In the version published online on June 27, 2013, the affiliations included a few errors. In addition, the author Violet Gelowani was accidently omitted from the author list. All of these mistakes have been corrected in the online and the print versions of the article and appear correctly here. The authors and The Journal regret the errors.

AB - (The American Journal of Human Genetics 93, 197–210; August 8, 2013) In the version published online on June 27, 2013, the affiliations included a few errors. In addition, the author Violet Gelowani was accidently omitted from the author list. All of these mistakes have been corrected in the online and the print versions of the article and appear correctly here. The authors and The Journal regret the errors.

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DO - 10.1016/j.ajhg.2013.07.001

M3 - Comment/debate

AN - SCOPUS:85123495204

SN - 0002-9297

VL - 93

SP - 405

JO - American journal of human genetics

JF - American journal of human genetics

IS - 2

ER -

Wiszniewski W, Hunter JV, Hanchard NA, Willer JR, Shaw C, Tian Q et al. Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027)). American journal of human genetics. 2013 Aug 8;93(2):405. doi: 10.1016/j.ajhg.2013.07.001

Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))

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