Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Fei Liu; Jiongjiong Hu; Wenjun Xia; Lili Hao; Jing Ma; Duan Ma; Zhaoxin Ma

doi:10.1371/journal.pone.0126602

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Open Access

Peer-reviewed

Research Article

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Fei Liu ,

Contributed equally to this work with: Fei Liu, Jiongjiong Hu

Affiliation Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China
⨯
Jiongjiong Hu ,

Contributed equally to this work with: Fei Liu, Jiongjiong Hu

Affiliation Department of Otorhinolaryngology, Shanghai East Hospital, Tongji University, Shanghai, China
⨯
Wenjun Xia,

Affiliation Institutes of Biomedical Sciences, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China
⨯
Lili Hao,

Affiliation Institutes of Biomedical Sciences, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China
⨯
Jing Ma,

Affiliation Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China
⨯
Duan Ma ,

* E-mail: duanma@fudan.edu.cn (DM); mzhx114@163.com (ZM)

Affiliations Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China, Institutes of Biomedical Sciences, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China
⨯
Zhaoxin Ma

* E-mail: duanma@fudan.edu.cn (DM); mzhx114@163.com (ZM)

Affiliation Department of Otorhinolaryngology, Shanghai East Hospital, Tongji University, Shanghai, China
⨯

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Fei Liu,
Jiongjiong Hu,
Wenjun Xia,
Lili Hao,
Jing Ma,
Duan Ma,
Zhaoxin Ma

Published: May 11, 2015
https://doi.org/10.1371/journal.pone.0126602

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