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Q30411037-49A8DF45-18BF-45CC-92B9-E8D2EF1BF708
Q30411037-49A8DF45-18BF-45CC-92B9-E8D2EF1BF708
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http://www.wikidata.org/entity/statement/Q30411037-49A8DF45-18BF-45CC-92B9-E8D2EF1BF708
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.
P2860
Q30411037-49A8DF45-18BF-45CC-92B9-E8D2EF1BF708
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30411037-49A8DF45-18BF-45CC-92B9-E8D2EF1BF708
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type
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Statement
wasDerivedFrom
112d2c1c06254e2561f2994a5e725f72a8b710e1
P2860
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene.