A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy (Q28299243)
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Current Data About A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
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(P1932) H Watkins
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(P1476) "A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy" (language: en)

(P2093) 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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(P813) Thursday, January 7, 2021
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(P813) Thursday, January 7, 2021
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(P813) Thursday, January 7, 2021
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External Links
(P356) 10.1038/NG0195-75
(P698) 7704029
(P5875) 15495201
(P6179) 1031902293