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Q46809494-D9ACE36F-6FCB-47F2-B9F4-D4B8DC918FD4
Q46809494-D9ACE36F-6FCB-47F2-B9F4-D4B8DC918FD4
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http://www.wikidata.org/entity/statement/Q46809494-D9ACE36F-6FCB-47F2-B9F4-D4B8DC918FD4
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
P2860
Q46809494-D9ACE36F-6FCB-47F2-B9F4-D4B8DC918FD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46809494-D9ACE36F-6FCB-47F2-B9F4-D4B8DC918FD4
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wasDerivedFrom
e148f11413fea8a7433a93ca2f6ebd2cb6b0b784
P2860
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children.