Clinical findings of a myoclonus-dystonia family with two distinct mutations

D. Doheny*, F. Danisi, C. Smith, C. Morrison, M. Velickovic, D. De Leon, S. B. Bressman, J. Leung, L. Ozelius, C. Klein, X. O. Breakefield, M. F. Brin, J. M. Silverman

*Korrespondierende/r Autor/-in für diese Arbeit
44 Zitate (Scopus)

Abstract

Myoclonus-dystonia has recently been associated with mutations in the epsilon-sarcoglycan gene (SCGE) on 7q21. Previously, the authors reported a patient with myoclonus-dystonia and an 18-bp deletion in the DYT1 gene on 9q34. The authors have now re-evaluated the patient harboring this deletion for mutations in the SGCE gene and identified a missense change. In the current study, the authors describe the clinical details of this family carrying mutations in two different dystonia genes. Further analysis of these mutations separately and together in cell culture and in animal models should clarify their functional consequences.

OriginalspracheEnglisch
ZeitschriftNeurology
Jahrgang59
Ausgabenummer8
Seiten (von - bis)1244-1246
Seitenumfang3
ISSN0028-3878
DOIs
PublikationsstatusVeröffentlicht - 22.10.2002

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