Myoclonus-Dystonia Syndrome

Open Access

|Nov 2002

Doheny DO Brin MF Morrison CE Smith CJ Walker RH Abbasi S Phenotypic features of myoclonus-dystonia in three kindreds Neurology 2002 Oct 59 8 1187 1196 10.1212/WNL.59.8.1187 12391346
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Grimes DA Han F Lang AE St George-Hyssop P Racacho L Bulman DE A novel locus for inherited myoclonus-dystonia on 18p11 Neurology 2002 Oct 59 8 1183 1186 10.1212/WNL.59.8.1183 12391345
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Doheny D Danisi F Smith C Morrison C Velickovic M De Leon D Clinical findings of a myoclonus-dystonia family with two distinct mutations Neurology 2002 Oct 59 8 1244 1246 10.1212/WNL.59.8.1187 12391355
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Leuzzi Y Carducci C Carducci C Cardona F Artiola C Antonozzi I Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome Neurology 2002 Oct 59 8 1241 1243 10.1212/WNL.59.8.1241 12391354
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Furukawa Y Rajput AH Inherited myoclonus-dystonia: how many causative genes and clinical phenotypes? Neurology 2002 Oct 59 8 1130 1131 10.1212/WNL.59.8.1130 12391338
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Language: English

Page range: 83 - 84

Published on: Nov 1, 2002

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

© 2002 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.