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 2017

Comprehensive analysis of syndromic hearing loss patients in Japan

por Ideura, Michie, Nishio, Shin-ya, Moteki, Hideaki, Takumi, Yutaka, Miyagawa, Maiko, Sato, Teruyuki, Kobayashi, Yumiko, Ohyama, Kenji, Oda, Kiyoshi, Matsui, Takamichi, Ito, Tsukasa, Suzumura, Hiroshi, Nagai, Kyoko, Izumi, Shuji, Nishiyama, Nobuhiro, Komori, Manabu, Kumakawa, Kozo, Takeda, Hidehiko, Kishimoto, Yoko, Iwasaki, Satoshi, Furutate, Sakiko, Ishikawa, Kotaro, Fujioka, Masato, Nakanishi, Hiroshi, Nakayama, Jun, Horie, Rie, Ohta, Yumi, Naito, Yasushi, Kakudo, Mariko, Sakaguchi, Hirofumi, Kataoka, Yuko, Sugahara, Kazuma, Hato, Naohito, Nakagawa, Takashi, Tsuchihashi, Nana, Kanda, Yukihiko, Kihara, Chiharu, Tono, Tetsuya, Miyanohara, Ikuyo, Ganaha, Akira, Usami, Shin-ichi
Publicado 2019