Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening

Takuya Yano, Shin Ya Nishio, Shin Ichi Usami, Norihito Takeichi, Satoshi Fukuda, Atsushi Namba, Hideichi Shinkawa, Yumiko Kobayashi, Hiroaki Sato, Tetsuaki Kawase, Toshimitsu Kobayashi, Tomoo Watanabe, Tsukasa Ito, Masaru Aoyagi, Hiroshi Ogawa, Koichi Omori, Kotaro Ishikawa, Keiichi Ichimura, Kyoko Nagai, Nobuhiko FuruyaShuntaro Shigihara, Yasuyuki Nomura, Minoru Ikeda, Tetsuo Ikezono, Toshiaki Yagi, Shunichi Tomiyama, Hiromi Kojima, Yuika Sakurai, Hiroshi Moriyama, Kozo Kumakawa, Hajime Sano, Makito Okamoto, Satoshi Iwasaki, Kazuhiko Takeuchi, Masako Nakai, Masahiko Higashikawa, Hiroshi Takenaka, Yuko Saito, Masafumi Sakagami, Yasushi Naito, Keiji Fujihara, Akihiro Sakai, Noboru Yamanaka, Kunihiro Fukushima, Kazunori Nishizaki, Kazuma Sugahara, Hiroshi Yamashita, Naoto Hato, Kiyofumi Gyo, Yasuhiro Kakazu, Shizuo Komune, Mayumi Sugamura, Takashi Nakagawa, Haruo Takahashi, Yukihiko Kanda, Hirokazu Kawano, Tetsuya Tono, Ikuyo Miyanohara, Yuichi Kurono, Akira Ganaha, Mikio Suzuki

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Medicine & Life Sciences