Phenotypic expressions of chronic leber's hereditary optic neuropathy patients with primary and secondary mitochondrial mutations presenting at tertiary eye care center, South India-Reference-Cited by-同舟云学术

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Phenotypic expressions of chronic leber's hereditary optic neuropathy patients with primary and secondary mitochondrial mutations presenting at tertiary eye care center, South India

Published:2022 Issue:1 Volume:9 Page:8
ISSN:2347-5617
Container-title:Egyptian Retina Journal
language:en
Short-container-title:Egypt Retina J

Author:

Challa NaveenKumar,Narsini HimaBindu,Aldakhil Sulaiman

Publisher

Medknow

Subject

Ocean Engineering

Reference21 articles.

1. Influence of mutation type on clinical expression of leber hereditary optic neuropathy;Spruijt;Am J Ophthalmol,2006

2. Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India;Khan;Invest Ophthalmol Vis Sci,2013

3. Leber hereditary optic neuropathy;Yu-Wai-Man;J Med Genet,2002

4. Demographics of a large international population of patients affected by leber's hereditary optic neuropathy;Poincenot;Ophthalmology,2020

5. Yu-Wai-Man P, Chinnery PF. Leber hereditary optic neuropathy. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews®. Seattle (WA): University of Washington, Seattle; 2000, 1993-2021.

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