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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Kitano T, et al. Among authors: nishiyama n.
PLoS One. 2017 May 17;12(5):e0177636. doi: 10.1371/journal.pone.0177636. eCollection 2017.
PLoS One. 2017.
PMID: 28545070
Free PMC article.