The mitochondrial tRNAThr G15930A may be a novel mutation associated with hearing impairment-Reference-Cited by-同舟云学术

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The mitochondrial tRNAThr G15930A may be a novel mutation associated with hearing impairment

Published:2019-01-02 Issue:1 Volume:4 Page:1347-1349
ISSN:2380-2359
Container-title:Mitochondrial DNA Part B
language:en
Short-container-title:Mitochondrial DNA Part B

Author:

Ding Yu¹,Liu Qi²,Teng Yao-Shu³,Zheng Hui¹,Leng Jian-Hang¹

Affiliation:

1. Central laboratory, Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, PR China;

2. Department of laboratory medicine, Shaoxing People’s Hospital, Shaoxing Hospital of Zhejiang University School of Medicine, Shaoxing, PR China;

3. Department of Otorhinolaryngology, Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, PR China

Funder

Hangzhou Health and Family Planning Commission

Ministry of Public Health of Zhejiang Province

Shaoxing Bureau of Science and Technology

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

https://tandfonline.com/doi/pdf/10.1080/23802359.2019.1597648

Reference12 articles.

1. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

2. Is mitochondrial tRNALeu(UUR)3291T>C mutation pathogenic?

3. Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

4. Mitochondrial tRNALeu(UUR) C3275T, tRNAGln T4363C and tRNALys A8343G mutations may be associated with PCOS and metabolic syndrome

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method;Bioscience Reports;2020-05

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