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UnknownMissense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.
Not available
S-EPMC2453783 | biostudies-literature
UnknownGenetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
Not available
S-EPMC1287932 | biostudies-literature
UnknownCDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
Not available
S-EPMC379159 | biostudies-literature
UnknownGJB2 mutations and degree of hearing loss: a multicenter study.
Not available
S-EPMC1285178 | biostudies-literature
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