A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1 (Q28296701)

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A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
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    A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1 (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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    H Watkins
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    June 1995
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    10
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    2
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    249
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