Mutation spectrum of nonâsyndromic hearing loss in the UAE, a retrospective cohort study and literature review
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DOI: 10.1002/mgg3.2052
Abstract: Hearing loss (HL) is a heterogeneous condition that causes partial or complete hearing impairment. Hundreds of variants in >60 genes have been reported to be associated with Hereditary HL (HHL), variants of the GJB2 gene… read more here.
Keywords: hearing loss; loss; non syndromic; mutation spectrum ... See more keywords