Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ɛ-sarcoglycan mutations-Reference-Cited by-同舟云学术

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ɛ-sarcoglycan mutations

Published:2008 Issue:4 Volume:23 Page:588-592
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Raymond Deborah,Saunders-Pullman Rachel,de Carvalho Aguiar Patricia,Schule Birgitt,Kock Norman,Friedman Jennifer,Harris Juliette,Ford Blair,Frucht Steven,Heiman Gary A.,Jennings Danna,Doheny Dana,Brin Mitchell F.,de Leon Brin Deborah,Multhaupt-Buell Trisha,Lang Anthony E.,Kurlan Roger,Klein Christine,Ozelius Laurie,Bressman Susan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference21 articles.

1. Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome

2. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

3. Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias

4. Myoclonus-dystonia syndrome: ε-sarcoglycan mutations and phenotype

5. Phenotypic features of myoclonus-dystonia in three kindreds

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