(Q28299243)

English

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

scientific article

Statements

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy (English)
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N G Laing
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S D Wilton
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P A Akkari
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S Dorosz
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K Boundy
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C Kneebone
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P Blumbergs
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S White
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January 1995
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9
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75-9
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1
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Identifiers

 
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