APA

Kitano T., Miyagawa M., Nishio S., Moteki H., Oda K., Ohyama K., Miyazaki H., Hidaka H., Nakamura K., Murata T., Matsuoka R., Ohta Y., Nishiyama N., Kumakawa K., Furutate S., Iwasaki S., Yamada T., Ohta Y., Uehara N., Noguchi Y. & Usami S. (20170915). POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. : PloS one.

Chicago

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 and Usami Shin-Ichi. 20170915. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. : PloS one.

Harvard

Kitano T., Miyagawa M., Nishio S., Moteki H., Oda K., Ohyama K., Miyazaki H., Hidaka H., Nakamura K., Murata T., Matsuoka R., Ohta Y., Nishiyama N., Kumakawa K., Furutate S., Iwasaki S., Yamada T., Ohta Y., Uehara N., Noguchi Y. and Usami S. (20170915). POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. : PloS one.

MLA

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 and Usami Shin-Ichi. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. : PloS one. 20170915.