Erratum: De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype (American Journal of Human Genetics (2016) 99(4) (991–999)(S0002929716303718)(10.1016/j.ajhg.2016.08.017))

Vandana Shashi*, Loren D M Pena, Katherine Kim, Barbara Burton, Maja Hempel, Kelly Schoch, Magdalena Walkiewicz, Heather M. McLaughlin, Megan Cho, Nicholas Stong, Scott E. Hickey, Christine M. Shuss, Michael S. Freemark, Jane S. Bellet, Martha Ann Keels, Melanie J. Bonner, Maysantoine El-Dairi, Megan Butler, Peter G. Kranz, Constance T R M StumpelSylvia Klinkenberg, Karin Oberndorff, Malik Alawi, Rene Santer, Slavé Petrovski, Outi Kuismin, Satu Korpi-Heikkilä, Olli Pietilainen, Palotie Aarno, Mitja I. Kurki, Alexander Hoischen, Anna C. Need, David B. Goldstein, Fanny Kortüm

*Corresponding author for this work

Research output: Contribution to journalComment/debate

5 Scopus citations

Abstract

(The American Journal of Human Genetics 99, 991–999; October 6, 2016) In the originally published version of this article, Table 1 unfortunately contained two errors: c.2472delC (p.Ser825Valfs18) should have been c.2472delC (p.Ser825Valfs16) (as correctly notated in the main text), and the title should have mentioned six individuals instead of four. The errors have been corrected online, and the authors apologize for any confusion.

Original languageEnglish (US)
Number of pages1
JournalAmerican journal of human genetics
Volume100
Issue number1
DOIs
StatePublished - Jan 5 2017

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Shashi, V., Pena, L. D. M., Kim, K., Burton, B., Hempel, M., Schoch, K., Walkiewicz, M., McLaughlin, H. M., Cho, M., Stong, N., Hickey, S. E., Shuss, C. M., Freemark, M. S., Bellet, J. S., Keels, M. A., Bonner, M. J., El-Dairi, M., Butler, M., Kranz, P. G., ... Kortüm, F. (2017). Erratum: De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype (American Journal of Human Genetics (2016) 99(4) (991–999)(S0002929716303718)(10.1016/j.ajhg.2016.08.017)). American journal of human genetics, 100(1). https://doi.org/10.1016/j.ajhg.2016.12.004