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Q35848621-59E6999B-10FF-4EDC-8A1D-3DFB9DFDB9AA
Q35848621-59E6999B-10FF-4EDC-8A1D-3DFB9DFDB9AA
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Statement
http://www.wikidata.org/entity/statement/Q35848621-59E6999B-10FF-4EDC-8A1D-3DFB9DFDB9AA
Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome.
P2860
Q35848621-59E6999B-10FF-4EDC-8A1D-3DFB9DFDB9AA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35848621-59E6999B-10FF-4EDC-8A1D-3DFB9DFDB9AA
rank
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wasDerivedFrom
7aed833393c986599857e0f53f1f69abbd71a249
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome