Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss-Reference-Cited by-同舟云学术

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Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss

Published:2020-03 Issue:13 Volume:99 Page:e19373
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Gao Zhen,Yuan Ya-Sheng

Funder

Youth Fund of National Natural Science Foundation of China

Training Program of Outstanding Academic Leaders of Shanghai Municipal Commission of Health and Family Planning

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference37 articles.

1. The role of mitochondrial DNA mutations in hearing loss;Ding;Biochem Genet,2013

2. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness;Prezant;Nat Genet,1993

3. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation;Tang;Gene,2007

4. The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness;Torroni;Am J Hum Genet,1999

5. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family;Zhao;Am J Hum Genet,2004

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1. Advances in gene therapy hold promise for treating hereditary hearing loss;Molecular Therapy;2023-04

2. Mitochondrial DNA is a major source of driver mutations in cancer;Trends in Cancer;2022-12

3. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29

4. Advancements in prevention and intervention of sensorineural hearing loss;Therapeutic Advances in Chronic Disease;2022-01

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