Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family
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DOI: 10.1007/s11033-017-4129-9
Abstract: In the present work, we identified two novel compound heterozygote mutations in the GPR98 (G protein-coupled receptor 98) gene causing Usher syndrome. Whole-exome sequencing was performed to study the genetic causes of Usher syndrome in… read more here.
Keywords: exome sequencing; novel compound; mutations gpr98; moroccan deaf ... See more keywords