Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

Open Access

Peer-reviewed

Research Article

Juanjuan Gao ,

Contributed equally to this work with: Juanjuan Gao, Qi Wang

Affiliation Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital, Beijing, China
⨯
Qi Wang ,

Contributed equally to this work with: Juanjuan Gao, Qi Wang

Affiliation Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital, Beijing, China
⨯
Cheng Dong,

Affiliation Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital, Beijing, China
⨯
Siqi Chen,

Affiliation Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital, Beijing, China
⨯
Yu Qi,

Affiliation Department of central laboratory, Peking University First Hospital, Beijing, China
⨯
Yuhe Liu

* E-mail: liuyuhefeng@163.com

Affiliation Department of Otolaryngology, Head and Neck Surgery, Peking University First Hospital, Beijing, China
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Deafness
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Cell cycle and cell division
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Autosomal dominant traits
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