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

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

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

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

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7663526 [ View in PubMed
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Polypeptides
NameUniProt ID
Tropomyosin alpha-3 chainP06753Details