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Q33816386-4EC55C2D-BC8B-4E69-9EA3-69680B494EFA
Q33816386-4EC55C2D-BC8B-4E69-9EA3-69680B494EFA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33816386-4EC55C2D-BC8B-4E69-9EA3-69680B494EFA
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
P2860
Q33816386-4EC55C2D-BC8B-4E69-9EA3-69680B494EFA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33816386-4EC55C2D-BC8B-4E69-9EA3-69680B494EFA
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Statement
wasDerivedFrom
b8e662c980a0709a7050ad63ce9f8dc4771310f9
P2860
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).