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

N G Laing; S D Wilton; P A Akkari; S Dorosz; K Boundy; C Kneebone; P Blumbergs; S White; H Watkins; D R Love

doi:10.1038/ng0195-75

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

Identifier:nobleid.org/w1/20260515/C5BABA00

Type:Journal Article

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

Identifier:nobleid.org/w1/20260515/C5BABA00

Type:Journal Article

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