Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations-Reference-Cited by-同舟云学术

Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations

Published:2021-04-08 Issue:4 Volume:42 Page:420-430
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Coussa Razek Georges¹^ORCID,Sohn Elliott H.¹,Han Ian C.¹,Parikh Sumit²,Traboulsi Elias I.³^ORCID

Affiliation:

1. Department of Ophthalmology and Visual Sciences, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA

2. Cleveland Clinic, Mitochondrial Medicine Center, Cleveland, Ohio, USA

3. Cleveland Clinic, Cole Eye Institute, Center for Genetic Eye Diseases, Cleveland, Ohio, USA

Funder

funding agencies in the public, commercial, or not-for-profit sectors

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2021.1907598

Reference92 articles.

1. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation

2. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

3. Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

4. Population prevalence of the MELAS A3243G mutation

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. Neuropathy, ataxia, retinitis pigmentosa: a case of a mother and two siblings;Ophthalmic Genetics;2023-09-06

2. Pathogenic mitochondrial DNA 3243A>G mutation: From genetics to phenotype;Frontiers in Genetics;2022-10-06

3. Mitochondrial Diabetes is Associated with tRNALeu(UUR) A3243G and ND6 T14502C Mutations;Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy;2022-06

4. Stargardt disease masquerades;Current Opinion in Ophthalmology;2021-02-26