Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation

Jennifer G Goldman; Sheila R. Eichenseer; Elizabeth Berry-Kravis; Simon Zimnowodzki; Allison Gregory; Penelope Hogarth; Susan J. Hayflick

doi:10.1002/mds.25410

Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation

Jennifer G Goldman^*, Sheila R. Eichenseer, Elizabeth Berry-Kravis, Simon Zimnowodzki, Allison Gregory, Penelope Hogarth, Susan J. Hayflick

^*Corresponding author for this work

Physical Medicine and Rehabilitation

Research output: Contribution to journal › Letter › peer-review

11 Scopus citations

Original language	English (US)
Pages (from-to)	1462-1463
Number of pages	2
Journal	Movement Disorders
Volume	28
Issue number	10
DOIs	https://doi.org/10.1002/mds.25410
State	Published - Sep 2013

ASJC Scopus subject areas

Clinical Neurology
Neurology

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10.1002/mds.25410

Cite this

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title = "Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation",

author = "Goldman, {Jennifer G} and Eichenseer, {Sheila R.} and Elizabeth Berry-Kravis and Simon Zimnowodzki and Allison Gregory and Penelope Hogarth and Hayflick, {Susan J.}",

year = "2013",

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volume = "28",

pages = "1462--1463",

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publisher = "John Wiley & Sons Inc.",

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AU - Goldman, Jennifer G

AU - Eichenseer, Sheila R.

AU - Berry-Kravis, Elizabeth

AU - Zimnowodzki, Simon

AU - Gregory, Allison

AU - Hogarth, Penelope

AU - Hayflick, Susan J.

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DO - 10.1002/mds.25410

M3 - Letter

C2 - 23494994

AN - SCOPUS:84884715844

SN - 0885-3185

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SP - 1462

EP - 1463

JO - Movement Disorders

JF - Movement Disorders

IS - 10

ER -

Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation

ASJC Scopus subject areas

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