LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
- 31 May 1998
- journal article
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 8 (3-4), 193-197
- https://doi.org/10.1016/s0960-8966(98)00014-5
Abstract
No abstract availableKeywords
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