Comment on

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

  Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029