POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing l...

Por 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
Publicado no PLoS One (2017)