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UnknownA truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.
Not available
S-EPMC6745279 | biostudies-literature
UnknownEvidence for genotype-phenotype correlation for OTOF mutations.
Not available
S-EPMC4066206 | biostudies-literature
UnknownMutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.
Not available
S-EPMC9245706 | biostudies-literature
UnknownVariations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.
Not available
S-EPMC4999867 | biostudies-literature
UnknownComprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Not available
S-EPMC4733433 | biostudies-literature
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