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Q24310222-7191D7E8-2E6F-454F-91F8-D2A75D8D4DC4
Q24310222-7191D7E8-2E6F-454F-91F8-D2A75D8D4DC4
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http://www.wikidata.org/entity/statement/Q24310222-7191D7E8-2E6F-454F-91F8-D2A75D8D4DC4
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
P2860
Q24310222-7191D7E8-2E6F-454F-91F8-D2A75D8D4DC4
BestRank
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http://www.wikidata.org/entity/statement/Q24310222-7191D7E8-2E6F-454F-91F8-D2A75D8D4DC4
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wasDerivedFrom
3a175361ac38de5ddaf741066b7242b5abb65ee3
P2860
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.