Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, Usami, Shin-ichi

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Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, Usami, Shin-ichi

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OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients von Iwasa, Yoh-Ichiro, Nishio, Shin-Ya, Sugaya, Akiko, Kataoka, Yuko, Kanda, Yukihiko, Taniguchi, Mirei, Nagai, Kyoko, Naito, Yasushi, Ikezono, Tetsuo, Horie, Rie, Sakurai, Yuika, Matsuoka, Rina, Takeda, Hidehiko, Abe, Satoko, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-Ya, Iwasaki, Satoshi, Takahashi, Masahiro, Ito, Tsukasa, Arai, Yasuhiro, Usami, Shin-Ichi

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Magnetic resonance imaging-based radiomics analysis of the differential diagnosis of ovarian clear cell carcinoma and endometrioid carcinoma: a retrospective study von Takeyama, Nobuyuki, Sasaki, Yasushi, Ueda, Yasuo, Tashiro, Yuki, Tanaka, Eliko, Nagai, Kyoko, Morioka, Miki, Ogawa, Takafumi, Tate, Genshu, Hashimoto, Toshi, Ohgiya, Yoshimitsu

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Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1 von Yoshimura, Hidekane, Iwasaki, Satoshi, Nishio, Shin-Ya, Kumakawa, Kozo, Tono, Tetsuya, Kobayashi, Yumiko, Sato, Hiroaki, Nagai, Kyoko, Ishikawa, Kotaro, Ikezono, Tetsuo, Naito, Yasushi, Fukushima, Kunihiro, Oshikawa, Chie, Kimitsuki, Takashi, Nakanishi, Hiroshi, Usami, Shin-Ichi

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Panhypopituitarism diagnosed in adulthood: Imaging findings of bone and other organs von Nagai, Kyoko, Sugimoto, Hideharu, Kachi, Mana, Tanaka, Eliko, Kigawa, Yasuyoshi, Tadokoro, Rie

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OTOF mutation screening in Japanese severe to profound recessive hearing loss patients von Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Kanda, Yukihiko, Kumakawa, Kozo, Abe, Satoko, Naito, Yasushi, Nagai, Kyoko, Usami, Shin-ichi

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Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns von Oguchi, Tomohiro, Ohtsuka, Akihiro, Hashimoto, Shigenari, Oshima, Aki, Abe, Satoko, Kobayashi, Yumiko, Nagai, Kyoko, Matsunaga, Tatsuo, Iwasaki, Satoshi, Nakagawa, Takashi, Usami, Shin-Ichi

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Congenital Arhinia: A Case Report and Functional Evaluation von Shino, Masato, Chikamatsu, Kazuaki, Yasuoka, Yoshihito, Nagai, Kyoko, Furuya, Nobuhiko

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The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B von Watanabe, Kizuki, Nishio, Shin-ya, Usami, Shin-ichi

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Comprehensive analysis of syndromic hearing loss patients in Japan von 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

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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study von Miyagawa, Maiko, Nishio, Shin-Ya, Usami, Shin-Ichi

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Collateral pulmonary vein after catheter ablation therapy for atrial fibrillation von Nagai, Kyoko, Kotake, Akio, Hori, Yoshiro, Takeyama, Nobuyuki, Tanaka, Eliko, Tashiro, Yuki, Hashimoto, Toshi, Wakatsuki, Daisuke, Suzuki, Hiroshi

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A large cohort study of GJB2 mutations in Japanese hearing loss patients von Tsukada, K, Nishio, S, Usami, S

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Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study von Usami, Shin-ichi, Nishio, Shin-ya, Nagano, Makoto, Abe, Satoko, Yamaguchi, Toshikazu

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Alternative Starting Position for CT Coronary Angiography von HORI, Yoshiro, KAWASAKI, Shota, NAKASHIMA, Junya, TASHIRO, Yuki, KOTAKE, Akio, NAGAI, Kyoko, TANAKA, Eliko, TAKEYAMA, Nobuyuki, HAYASHI, Takaki, HASHIMOTO, Toshi

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Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening von Yano, Takuya, Nishio, Shin-ya, Usami, Shin-ichi

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Hearing aid fitting for elderly hearing impaired at our clinic von Nagai, Kyoko, Kogure, Yuki, Kimura, Nanako, Suzuki, Satoru, Chiyoda, Tomoko, Mizutani, Kiyotaka, Tomaki, Kenichi

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Problem and Assignment for Distinguishing the Usher Syndrome Type von Iwasaki, Satoshi, Yoshimura, Hidekane, Takeichi, Norito, Satou, Hiroaki, Ishikawa, Kotaro, Kaga, Kimitaka, Kumakawa, Kozou, Nagai, Kyoko, Furuya, Nobuhiko, Ikezono, Tetsuo, Nakanishi, Hiroshi, Naitou, Yasu, Fukushima, Kunihiro, Tono, Tetsuya, Kimitsuki, Takashi, Nishio, Shinya, Takumi, Yutaka, Usami, Shinichi

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Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations von Suzuki, Hiroaki, Oshima, Aki, Tsukamoto, Koji, Abe, Satoko, Kumakawa, Kozo, Nagai, Kyoko, Satoh, Hitoshi, Kanda, Yukihiko, Iwasaki, Satoshi, Usami, Shin-ichi

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