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    Nat Genet. 1995 Jun;10(2):249.

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

    Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al.

    Erratum for:

    PMID: 7663526 [PubMed - indexed for MEDLINE]

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