Missense mutations in desmin associated with familial cardiac and skeletal myopathy
(Q24322607)
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Missense mutations in desmin associated with familial cardiac and skeletal myopathy
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(P356) |
10.1038/1300
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(P698) |
9697706
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(P3181) |
4156665
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(P5875) |
13586976
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(P6179) |
1045674591
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