Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan (Human Genetics, (2022), 141, 3-4, (865-875), 10.1007/s00439-021-02351-7)

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

研究成果: ジャーナルへの寄稿コメント/討論査読

抄録

In the original article published, there is a correction in Table 1. We would like to remove the variant (c.4023 + 1G > A) from the Table. The correct Table 1 is attached below. The original article has been corrected.

本文言語英語
ページ(範囲)993-995
ページ数3
ジャーナルHuman Genetics
141
3-4
DOI
出版ステータス出版済み - 4月 2022
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 遺伝学
  • 遺伝学(臨床)

フィンガープリント

「Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan (Human Genetics, (2022), 141, 3-4, (865-875), 10.1007/s00439-021-02351-7)」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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