A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
(Q34411392)
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A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
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External Links
| (P356) |
10.1038/NATURE03467
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| (P698) |
15829955
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| (P6179) |
1038943070
|