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

*Corresponding author for this work
44 Citations (Scopus)


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.

Original languageEnglish
Issue number8
Pages (from-to)1244-1246
Number of pages3
Publication statusPublished - 22.10.2002


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