Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype—The importance of dystrophin and molecular genetic analysis
- 31 December 1992
- journal article
- case report
- Published by Elsevier in Neuromuscular Disorders
- Vol. 2 (2) , 121-124
- https://doi.org/10.1016/0960-8966(92)90044-7
Abstract
No abstract availableKeywords
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