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Q34325410-F4EF7A57-140D-4F9D-A4A3-6FF3ADBC449F
Q34325410-F4EF7A57-140D-4F9D-A4A3-6FF3ADBC449F
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Statement
http://www.wikidata.org/entity/statement/Q34325410-F4EF7A57-140D-4F9D-A4A3-6FF3ADBC449F
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).
P2860
Q34325410-F4EF7A57-140D-4F9D-A4A3-6FF3ADBC449F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34325410-F4EF7A57-140D-4F9D-A4A3-6FF3ADBC449F
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wasDerivedFrom
5e9ad829de6fc7ea2658d53f95e8bda703e0385d
P2860
Identification of cis-element regulating expression of the mouse Fgf10 gene during inner ear development