Increased Risk of Sensorineural Hearing Loss and Migraine in Patients With a Rare Mitochondrial DNA Variant 4336A>G in tRNAGln

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.38.6.400
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

AUDIOLOGY JAPAN
2003English

Lack of a Modulative Factor in Locus 8p23 in a Finnish Family With Nonsyndromic Sensorineural Hearing Loss Associated With the 1555A>G Mitochondrial DNA Mutation

European Journal of Human Genetics
Genetics
2003English

Mean Platelet Volume in Patients With Sensorineural Hearing Loss

Journal of Laryngology and Otology
MedicineOtorhinolaryngology
2014English

Frequency and Clinical Features of Patients With Sensorineural Hearing Loss Associated With the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics

Journal of Human Genetics
Genetics
2001English

Sensorineural Hearing Loss

Otology and Neurotology
MedicineOtorhinolaryngologySensory SystemsNeurology
2013English

Non Infectious Risk Factors in Pediatric Sensorineural Hearing Loss

Journal of thee Medical Sciences (Berkala Ilmu Kedokteran)
2017English

Sensorineural Hearing Loss

2007English

Sensorineural Hearing Loss

Journal of Clinical Rheumatology
MedicineRheumatology
2010English

Acute Sensorineural Hearing Loss

Acta Oto-Laryngologica
MedicineOtorhinolaryngology
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy