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Q38673397-48DFD967-60E4-4D31-871E-E3AD71E876ED
Q38673397-48DFD967-60E4-4D31-871E-E3AD71E876ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38673397-48DFD967-60E4-4D31-871E-E3AD71E876ED
Molecular diagnostics for hereditary hearing loss in children.
P2860
Q38673397-48DFD967-60E4-4D31-871E-E3AD71E876ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38673397-48DFD967-60E4-4D31-871E-E3AD71E876ED
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wasDerivedFrom
b8166dd02a7a4834aa4cd6cdb5ff4a9931f4829a
P2860
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3