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GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss.
Zheng, Jing; Ying, Zhengbiao; Cai, Zhaoyang; Sun, Dongmei; He, Zheyun; Gao, Yinglong; Zhang, Ting; Zhu, Yi; Chen, Ye; Guan, Min-Xin.
Affiliation
  • Zheng J; Institute of Genetics, School of Medicine, Zhejiang University, Hangzhou, China.
  • Ying Z; Department of Otolaryngology, Wenling People's Hospital, Wenzhou Medical University, Taizhou, China.
  • Cai Z; Department of Otolaryngology, Wenling People's Hospital, Wenzhou Medical University, Taizhou, China.
  • Sun D; Department of Laboratory Medicine, Jinhua Municipal Central Hospital, Jinhua, China.
  • He Z; Attardi Institute of Mitochondrial Biomedicine, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
  • Gao Y; Attardi Institute of Mitochondrial Biomedicine, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
  • Zhang T; Department of Otolaryngology, Wenling People's Hospital, Wenzhou Medical University, Taizhou, China.
  • Zhu Y; Department of Otolaryngology, the First Affiliated Hospital, Wenzhou Medical University, Wenzhou, China.
  • Chen Y; Institute of Genetics, School of Medicine, Zhejiang University, Hangzhou, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou, China.
  • Guan MX; Institute of Genetics, School of Medicine, Zhejiang University, Hangzhou, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou, China.
PLoS One ; 10(6): e0128691, 2015.
Article in En | MEDLINE | ID: mdl-26043044
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ethnicity / Connexins / Asian People / Genetic Association Studies / Hearing Loss / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
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PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ethnicity / Connexins / Asian People / Genetic Association Studies / Hearing Loss / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country: