POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
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DOI: 10.1371/journal.pone.0177636
Abstract: A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic hereditary hearing loss, DFNA15. To date, 14 variants, including a whole deletion of POU4F3, have been reported to cause HL in… read more here.
Keywords: japanese hearing; hearing loss; pou4f3; autosomal dominant ... See more keywords