Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS

Open Access

Peer-reviewed

Research Article

Maiko Miyagawa,

Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
⨯
Shin-ya Nishio,

Affiliation Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan
⨯
Takuo Ikeda,

Affiliation Department of Otolaryngology, Tsudumigaura Handicapped Children’s Hospital, Shunan, Japan
⨯
Kunihiro Fukushima,

Affiliation Department of Otorhinolaryngology, Okayama University School of Medicine, Okayama, Japan
⨯
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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Deafness
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Frameshift mutation
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Nonsense mutation
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Computer software
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Mutation
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Etiology
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Hearing disorders
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Heterozygosity
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