POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
日本听力损失患者POU4F3基因突变筛查:基于大规模平行DNA测序的分析发现了与常染色体显性遗传性听力损失相关的新变异
期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0177636
Kitano, Tomohiro; Miyagawa, Maiko; Nishio, Shin-Ya; Moteki, Hideaki; Oda, Kiyoshi; Ohyama, Kenji; Miyazaki, Hiromitsu; Hidaka, Hiroshi; Nakamura, Ken-Ichi; Murata, Takaaki; Matsuoka, Rina; Ohta, Yoko; Nishiyama, Nobuhiro; Kumakawa, Kozo; Furutate, Sakiko; Iwasaki, Satoshi; Yamada, Takechiyo; Ohta, Yumi; Uehara, Natsumi; Noguchi, Yoshihiro; Usami, Shin-Ichi