Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction-Reference-Cited by-同舟云学术

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Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction

Published:2016-03-25 Issue:6 Volume:139 Page:e34-e34
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Santarelli Rosamaria,Cama Elona,Scimemi Pietro,La Morgia Chiara,Caporali Leonardo,Valentino Maria Lucia,Liguori Rocco,Carelli Valerio

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/139/6/e34/

Reference12 articles.

1. Mitochondrial DNA: Impacting Central and Peripheral Nervous Systems

2. The spectrum of hearing loss due to mitochondrial DNA defects

3. Are inner or outer hair cells the source of summating potentials recorded from the round window?

4. Abnormal brainstem auditory evoked responses in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Evidence of delayed central conduction time

5. Psychophysical Evaluation of Cochlear Hair Cell Damage Due to the A3243G Mitochondrial DNA Mutation

Cited by 5 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. Neuro‐Otology;Neurology;2024-03-15

2. The Importance of Mitochondrial Disease Testing in Young Adults With New Onset Sensorineural Hearing Loss;Ear & Hearing;2023-11-06

3. Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy;Frontiers in Neuroscience;2019-05-28

4. Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review;Orphanet Journal of Rare Diseases;2018-02-21

5. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society;Genetics in Medicine;2017-12

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