A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
- PMID: 7663526
- DOI: 10.1038/ng0695-249
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
Erratum for
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A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029
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