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Inherited eye-related disorders due to mitochondrial dysfunction

Published:2017-05-08 Issue:R1 Volume:26 Page:R12-R20
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Yu-Wai-Man Patrick¹²³,Newman Nancy J.⁴

Affiliation:

1. Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK

2. NIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK

3. Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK

4. Departments of Ophthalmology, Neurology and Neurological Surgery, Emory University School of Medicine, Atlanta, GA, USA

Funder

NIH

NEI

National Institute of Health Research (NIHR)

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/R1/R12/25421218/ddx182.pdf

Reference80 articles.

1. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease;Gorman;Ann. Neurol,2015

2. Monogenic mitochondrial disorders;Koopman;N. Eng. J. Med,2012

3. Mutations causing mitochondrial disease: What is new and what challenges remain?;Lightowlers;Science,2015

4. Disturbed mitochondrial dynamics and neurodegenerative disorders;Burte;Na. Rev. Neurol,2015

5. The neuro-ophthalmology of mitochondrial disease;Fraser;Surv. Ophthalmol,2010

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