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Q55387725-EE4A9A40-BD70-464A-B11D-7A6DFD7F9243
Q55387725-EE4A9A40-BD70-464A-B11D-7A6DFD7F9243
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http://www.wikidata.org/entity/statement/Q55387725-EE4A9A40-BD70-464A-B11D-7A6DFD7F9243
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
P2860
Q55387725-EE4A9A40-BD70-464A-B11D-7A6DFD7F9243
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http://www.wikidata.org/entity/statement/Q55387725-EE4A9A40-BD70-464A-B11D-7A6DFD7F9243
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wasDerivedFrom
1e141fa3fbe0ba6eacc0c8725f25636f4663eb85
P2860
Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.