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Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 4, p. 500, doi. 10.1002/ana.23831
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- Article
Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H.
- Published in:
- Human Mutation, 2009, v. 30, n. 9, p. E831, doi. 10.1002/humu.21063
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- Publication type:
- Article
Genetic linkage of Welander distal myopathy to chromosome 2p13.
- Published in:
- Annals of Neurology, 1999, v. 46, n. 3, p. 399, doi. 10.1002/1531-8249(199909)46:3<399::AID-ANA16>3.0.CO;2-Q
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- Article