Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA <sup>Ala</sup> 5601C>T and tRNA <sup>Leu(CUN)</sup> 12311T>C mutations-Reference-Cited by-同舟云学术

Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA ^Ala 5601C>T and tRNA ^Leu(CUN) 12311T>C mutations

Published:2022-02-26 Issue:4 Volume:36 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:Clinical Laboratory Analysis

Author:

Yu Xuejiao¹,Li Sheng²,Ding Yu³^ORCID

Affiliation:

1. Department of Clinical Laboratory Quzhou People's Hospital the Quzhou Affiliated Hospital of Wenzhou Medical University Quzhou China

2. Department of Otolaryngology Quzhou People's Hospital the Quzhou Affiliated Hospital of Wenzhou Medical University Quzhou China

3. Central Laboratory Hangzhou First People’s Hospital Zhejiang University School of Medicine Hangzhou China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.24298

Reference70 articles.

1. Human Nonsyndromic Sensorineural Deafness

2. Hereditary deafness and phenotyping in humans

3. Genetic Causes of Hearing Loss

4. Connexin26 Mutations Associated With Nonsyndromic Hearing Loss

5. Deafness Gene Mutations in Newborns in the Foshan Area of South China With Bloodspot-Based Genetic Screening Tests

Cited by 4 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. The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control Study;Pharmacogenomics and Personalized Medicine;2024-03

2. Mitochondrial Diabetes Is Associated with the ND4 G11696A Mutation;Biomolecules;2023-05-30

3. 4‐octyl itaconate improves the viability of D66H cells by regulating the KEAP1‐NRF2‐GCLC/HO‐1 pathway;Journal of Cellular and Molecular Medicine;2023-03-13

4. Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness;Genes;2022-10-05