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Q46809494-EF92320D-568C-4626-A9B1-4D2D07A0194D
Q46809494-EF92320D-568C-4626-A9B1-4D2D07A0194D
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http://www.wikidata.org/entity/statement/Q46809494-EF92320D-568C-4626-A9B1-4D2D07A0194D
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
P2860
Q46809494-EF92320D-568C-4626-A9B1-4D2D07A0194D
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Statement
http://www.wikidata.org/entity/statement/Q46809494-EF92320D-568C-4626-A9B1-4D2D07A0194D
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wasDerivedFrom
e148f11413fea8a7433a93ca2f6ebd2cb6b0b784
P2860
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.