De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay

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Bibliographic Details
Published inMovement disorders Vol. 30; no. 9; pp. 1290 - 1292
Main Authors Zhang, Zhong-Bin, Tian, Mao-Qiang, Gao, Kai, Jiang, Yu-Wu, Wu, Ye
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.08.2015
Wiley Subscription Services, Inc
Subjects
Child, Preschool
Chorea - genetics
Developmental Disabilities - genetics
Humans
Large-Conductance Calcium-Activated Potassium Channel alpha Subunits - genetics
Male
Movement disorders
Mutation - genetics
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Bibliography:Peking University First Hospital
ArticleID:MDS26216
istex:676D29C4D0617FFAF4D60D21338843DBBE9AA35F
ark:/67375/WNG-VL4LHRVX-5
Full financial disclosures and author roles may be found in the online version of this article.
These authors contributed equally to this work.
Nothing to report.
Relevant conflicts of interest/financial disclosures
Funding agencies
The study was supported by the National Key Technology R&D program (2012BAI09B00), and the Key Laboratory Program of the Ministry of Education (2012‐RG/ND‐0001).
ISSN:0885-3185
1531-8257
DOI:10.1002/mds.26216