ε-sarcoglycan mutations found in combination with other dystonia gene mutations

Author:

Klein Christine,Liu Liu,Doheny Dana,Kock Norman,Müller Birgitt,De Carvalho Aguiar Patricia,Leung Joanne,De Leon Deborah,Bressman Susan B.,Silverman Jeremy,Smith Christopher,Danisi Fabio,Morrison Chris,Walker Ruth H.,Velickovic Miodrag,Schwinger Eberhard,Kramer Patricia L.,Breakefield Xandra O.,Brin Mitchell F.,Ozelius Laurie J.

Funder

Fritz Thyssen Foundation

Deutsche Forschungsgemeinschaft

Myoclonus Foundation

Dystonia Medical Research Foundation

Bachmann-Strauss Dystonia and Parkinson Foundation, Inc.

CAPES Foundation

NINDS

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Inherited myoclonus-dystonia syndrome;Gasser;Adv Neurol,1998

2. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31;Nygaard;Ann Neurol,1999

3. A major locus for myoclonus-dystonia maps to chromosome 7q in eight families;Klein;Am J Hum Genet,2000

4. A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q;Vidailhet;Neurology,2001

5. Inherited myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families;Asmus;Ann Neurol,2001

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