Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome
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Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome
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(P356) |
10.1038/NG1775
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(P698) |
16642020
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(P3181) |
3908209
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(P5875) |
7139165
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(P6179) |
1025751715
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