Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation

• Takehiko Naito,

  Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan

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• Shin-ya Nishio,

  Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan

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• Yoh-ichiro Iwasa,

  Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan

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• Takuya Yano,

  Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan

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• Kozo Kumakawa,

  Affiliation Department of Otolaryngology, Toranomon Hospital, Tokyo, Japan

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• Satoko Abe,

  Affiliation Department of Otolaryngology, Toranomon Hospital, Tokyo, Japan

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• Kotaro Ishikawa,

  Affiliation Department of Otorhinolaryngology, Jichi Medical University, Tochigi, Japan

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• Hiromi Kojima,

  Affiliation Department of Otorhinolaryngology, Jikei University School of Medicine, Tokyo, Japan

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• Atsushi Namba,

  Affiliation Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki, Japan

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• Chie Oshikawa,

  Affiliation Department of Otorhinolaryngology, Kyushu University School of Medicine, Fukuoka, Japan

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• Shin-ichi Usami

  * E-mail: usami@shinshu-u.ac.jp

  Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan

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