STXBP1 Stop‐Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy

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Bibliographic Details
Published inMovement disorders clinical practice (Hoboken, N.J.) Vol. 9; no. 6; pp. 837 - 840
Main Authors Spaull, Robert, Steel, Dora, Barwick, Katy, Prabhakar, Prab, Wakeling, Emma, Kurian, Manju A.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.08.2022
Wiley Subscription Services, Inc
Subjects
Letters: Genotype and Phenotype
movement disorder
stop‐loss
STXBP1
tremor
Online AccessGet full text
ISSN2330-1619
2330-1619
DOI10.1002/mdc3.13509

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ISSN:2330-1619
2330-1619
DOI:10.1002/mdc3.13509