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Q30367238-0EF2D95E-5579-4A18-B720-79CBE83497AE
Q30367238-0EF2D95E-5579-4A18-B720-79CBE83497AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30367238-0EF2D95E-5579-4A18-B720-79CBE83497AE
Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.
P2860
Q30367238-0EF2D95E-5579-4A18-B720-79CBE83497AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30367238-0EF2D95E-5579-4A18-B720-79CBE83497AE
rank
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Statement
wasDerivedFrom
3a344e139dbc666a946e0032a5b1a25c45cc1ad4
P2860
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3