The mitochondrial COI/tRNASER(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family
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29. Dez. 2017
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Artikel-Kategorie: Original Article
Online veröffentlicht: 29. Dez. 2017
Seitenbereich: 43 - 49
DOI: https://doi.org/10.1515/bjmg-2017-0025
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© 2017 Ding Y, Xia B-H, Teng Y-S, Zhuo G-C, Leng J-H, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Ding, Y
Central Laboratory, Hangzhou First People’s HospitalHangzhou, People’s Republic of China
Affiliated Hangzhou Hospital, Nanjing Medical UniversityHangzhou, People’s Republic of China
Xia, B-H
Department of Pharmacy, Hunan Chinese Medical UniversityChangsha, People’s Republic of China
Teng, Y-S
Affiliated Hangzhou Hospital, Nanjing Medical UniversityHangzhou, People’s Republic of China
Department of Otolaryngology, Hangzhou First People’s HospitalHangzhou, People’s Republic of China
Zhuo, G-C
Central Laboratory, Hangzhou First People’s HospitalHangzhou, People’s Republic of China
Affiliated Hangzhou Hospital, Nanjing Medical UniversityHangzhou, People’s Republic of China
Leng, J-H
Central Laboratory, Hangzhou First People’s HospitalHangzhou, People’s Republic of China
Affiliated Hangzhou Hospital, Nanjing Medical UniversityHangzhou, People’s Republic of China