Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutations
- 13 April 2004
- journal article
- Published by Wolters Kluwer Health in Neurology
- Vol. 62 (7) , 1229-1231
- https://doi.org/10.1212/01.wnl.0000118286.75059.35
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Myoclonus–dystonia syndrome: ε‐sarcoglycan mutations and phenotypeAnnals of Neurology, 2002
- Book ReviewHormone Research in Paediatrics, 2002
- Myoclonus dystoniaNeurology, 2002
- Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndromeNature Genetics, 2001