Variants of human CLDN9 cause mild to profound hearing loss
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DOI: 10.1002/humu.24260
Abstract: Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent onset. Exome sequencing… read more here.
Keywords: hearing loss; cldn9; mild profound; deafness ... See more keywords