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

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

Published:2016-03-25 Issue:6 Volume:139 Page:e33-e33
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Kullar Peter J.,Quail Jenna,Lindsey Phillip,Wilson Janet A.,Horvath Rita,Yu-Wai-Man Patrick,Gorman Grainne S.,Taylor Robert W.,Ng Yi,McFarland Robert,Moore Brian C. J.,Chinnery Patrick F.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/139/6/e33/6697034/aww051.pdf

Reference13 articles.

1. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

2. Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy

3. Establishment of normative data for monaural recordings of auditory brainstem response and its application in screening patients with hearing loss: a cohort study;Chalak;J Clin Diagn Res,2013

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

5. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

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