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We describe 3 children with a similar clinical picture of autosomal dominant M\u2010D and an\n                    <jats:italic>SGCE<\/jats:italic>\n                    mutation in only one of them, suggesting that M\u2010D is genetically heterogeneous. \u00a9 2003 Movement Disorder Society\n                  <\/jats:p>","DOI":"10.1002\/mds.10635","type":"journal-article","created":{"date-parts":[[2004,2,17]],"date-time":"2004-02-17T04:00:27Z","timestamp":1076990427000},"page":"231-234","source":"Crossref","is-referenced-by-count":17,"title":["Clinical and genetic features of myoclonus\u2013dystonia in 3 cases: A video 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