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Q55387725-01C42011-8991-407E-B6DB-57256D9D43C2
Q55387725-01C42011-8991-407E-B6DB-57256D9D43C2
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http://www.wikidata.org/entity/statement/Q55387725-01C42011-8991-407E-B6DB-57256D9D43C2
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
P2860
Q55387725-01C42011-8991-407E-B6DB-57256D9D43C2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55387725-01C42011-8991-407E-B6DB-57256D9D43C2
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Statement
wasDerivedFrom
ddeeaa11e804e1f1a8e34180ba279852915ade2f
P2860
Usher syndrome: definition and estimate of prevalence from two high-risk populations.