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Q41035989-8A0D6D33-5B03-4C6E-92D0-36680BFBB768
Q41035989-8A0D6D33-5B03-4C6E-92D0-36680BFBB768
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41035989-8A0D6D33-5B03-4C6E-92D0-36680BFBB768
FGFR3 deficient mice have accelerated fracture repair.
P2860
Q41035989-8A0D6D33-5B03-4C6E-92D0-36680BFBB768
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41035989-8A0D6D33-5B03-4C6E-92D0-36680BFBB768
rank
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type
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wasDerivedFrom
b41cce23a28235e7bd9b44abcbf79ef15616fdce
P2860
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome