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Q28261525-1399BBC3-C67B-40BD-AB0E-76F6DCE0C0AC
Q28261525-1399BBC3-C67B-40BD-AB0E-76F6DCE0C0AC
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http://www.wikidata.org/entity/statement/Q28261525-1399BBC3-C67B-40BD-AB0E-76F6DCE0C0AC
Advances in Skeletal Dysplasia Genetics
P2860
Q28261525-1399BBC3-C67B-40BD-AB0E-76F6DCE0C0AC
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http://www.wikidata.org/entity/statement/Q28261525-1399BBC3-C67B-40BD-AB0E-76F6DCE0C0AC
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wasDerivedFrom
8b366e6d45a2710004ada62af1bf872aacef86c1
P2860
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.