Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation-Reference-Cited by-同舟云学术

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Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation

Published:1996-07-01 Issue:7 Volume:5 Page:963-971
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Guan M.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Cited by 197 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. High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect;Scientific Reports;2024-07-03

2. Aminoglycosides-Related Ototoxicity: Mechanisms, Risk Factors, and Prevention in Pediatric Patients;Pharmaceuticals;2023-09-25

3. Role of mitochondrial dysfunction and oxidative stress in sensorineural hearing loss;Hearing Research;2023-07

4. Our current understanding of the toxicity of altered mito-ribosomal fidelity during mitochondrial protein synthesis: What can it tell us about human disease?;Frontiers in Physiology;2023-06-30

5. Structural analysis of mitochondrial rRNA gene variants identified in patients with deafness;Frontiers in Physiology;2023-06-08

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