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Q35048191-4B10C3D2-7EA1-4596-A21F-9816AFF99467
Q35048191-4B10C3D2-7EA1-4596-A21F-9816AFF99467
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http://www.wikidata.org/entity/statement/Q35048191-4B10C3D2-7EA1-4596-A21F-9816AFF99467
SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).
P2860
Q35048191-4B10C3D2-7EA1-4596-A21F-9816AFF99467
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35048191-4B10C3D2-7EA1-4596-A21F-9816AFF99467
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wasDerivedFrom
e080c9e4c78fc638c434baa1ebfe6056a01698fb
P2860
The DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activity