Audiologic and Genetic Features of the A3243G mtDNA Mutation
Author:
Affiliation:
1. Department of Otolaryngology, University of Miami Ear Institute, Miami, Florida.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical),General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2012.0403
Reference32 articles.
1. The spectrum of hearing loss due to mitochondrial DNA defects
2. Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
3. The epidemiology of pathogenic mitochondrial DNA mutations
4. No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
5. Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
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1. Mitochondrial Diabetes is Associated with tRNALeu(UUR) A3243G and ND6 T14502C Mutations;Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy;2022-06
2. Response: Commentary: Neuromuscular and Muscle Metabolic Functions in MELAS Before and After Resistance Training: A Case Study;Frontiers in Physiology;2020-04-15
3. In Response to the Letter to the Editor: Auditory and Vestibular Dysfunction in M. 3243A>G Carriers;Otology & Neurotology;2019-10
4. Audiological and Vestibular Findings in Subjects with MELAS Syndrome;The Journal of International Advanced Otology;2019-08-15
5. Progression of Peripheral Vestibular Dysfunctions in Patients With a Mitochondrial A3243G Mutation;Otology & Neurotology;2019-03
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