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Q58765599-9FC7F69D-D88E-47EB-A36E-B68B486C8B40
Q58765599-9FC7F69D-D88E-47EB-A36E-B68B486C8B40
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http://www.wikidata.org/entity/statement/Q58765599-9FC7F69D-D88E-47EB-A36E-B68B486C8B40
Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families
P2860
Q58765599-9FC7F69D-D88E-47EB-A36E-B68B486C8B40
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Statement
http://www.wikidata.org/entity/statement/Q58765599-9FC7F69D-D88E-47EB-A36E-B68B486C8B40
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wasDerivedFrom
6ac43f68fcd5004e68545bae6c2cc028a5317b0b
P2860
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3