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Q46809494-A9D9BE47-C558-4A86-BE7D-97558B9F6ACD
Q46809494-A9D9BE47-C558-4A86-BE7D-97558B9F6ACD
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Statement
http://www.wikidata.org/entity/statement/Q46809494-A9D9BE47-C558-4A86-BE7D-97558B9F6ACD
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
P2860
Q46809494-A9D9BE47-C558-4A86-BE7D-97558B9F6ACD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46809494-A9D9BE47-C558-4A86-BE7D-97558B9F6ACD
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wasDerivedFrom
e148f11413fea8a7433a93ca2f6ebd2cb6b0b784
P2860
A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II.