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Q38214755-1CA0A127-BA36-4265-BE26-AB7997742797
Q38214755-1CA0A127-BA36-4265-BE26-AB7997742797
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http://www.wikidata.org/entity/statement/Q38214755-1CA0A127-BA36-4265-BE26-AB7997742797
Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss.
P2860
Q38214755-1CA0A127-BA36-4265-BE26-AB7997742797
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38214755-1CA0A127-BA36-4265-BE26-AB7997742797
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wasDerivedFrom
a74e84d10c0b010d90b207817739ec9d9f98cd7f
P2860
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA