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Q35042862-3B3A0C98-B255-461C-8685-C225E66EC03D
Q35042862-3B3A0C98-B255-461C-8685-C225E66EC03D
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http://www.wikidata.org/entity/statement/Q35042862-3B3A0C98-B255-461C-8685-C225E66EC03D
A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes.
P2860
Q35042862-3B3A0C98-B255-461C-8685-C225E66EC03D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35042862-3B3A0C98-B255-461C-8685-C225E66EC03D
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wasDerivedFrom
9f94608ac0f260a9fd23c4c7eeeaccff74417d07
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome