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The mitochondrial COI/tRNASER(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family Cover

The mitochondrial COI/tRNASER(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family

Balkan Journal of Medical Genetics
Volume 20 (2017): Issue 2 (December 2017)
By: Y Ding,  B-H Xia,  Y-S Teng,  G-C Zhuo and  J-H Leng  
Open Access
|Dec 2017
DOI: https://doi.org/10.1515/bjmg-2017-0025 | Journal eISSN: 2199-5761
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Language: English
Page range: 43 - 49
Published on: Dec 29, 2017
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
C1494T,
G7444A,
Chinese family,
Deafness,
Mitochondrial DNA (mtDNA),
Pathogenic variants
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2017 Y Ding, B-H Xia, Y-S Teng, G-C Zhuo, J-H Leng, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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