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Q24680303-E4E78055-6E66-4AAD-88D9-57610B7FE5A8
Q24680303-E4E78055-6E66-4AAD-88D9-57610B7FE5A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24680303-E4E78055-6E66-4AAD-88D9-57610B7FE5A8
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
P2860
Q24680303-E4E78055-6E66-4AAD-88D9-57610B7FE5A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24680303-E4E78055-6E66-4AAD-88D9-57610B7FE5A8
rank
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type
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Statement
wasDerivedFrom
e3409022898953331a913cd06da1a1bbc111d10c
P2860
Mutations in different components of FGF signaling in LADD syndrome.