A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1

Nat Genet. 1995 Jun;10(2):249. doi: 10.1038/ng0695-249.
No abstract available

Publication types

  • Published Erratum

MeSH terms

  • Base Sequence
  • Humans
  • Molecular Sequence Data
  • Tropomyosin / genetics*

Substances

  • Tropomyosin