Cargando…

Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation

Detalles Bibliográficos
Autores principales: Malhotra, Ravinder Mohan, Al Mejally, Mousa Ali, Abualela, Hanadi Mahmoud, Eltemamy, Marwa Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341278/
https://www.ncbi.nlm.nih.gov/pubmed/28298852
http://dx.doi.org/10.4103/0972-2327.194314
_version_ 1782512959102124032
author Malhotra, Ravinder Mohan
Al Mejally, Mousa Ali
Abualela, Hanadi Mahmoud
Eltemamy, Marwa Ahmed
author_facet Malhotra, Ravinder Mohan
Al Mejally, Mousa Ali
Abualela, Hanadi Mahmoud
Eltemamy, Marwa Ahmed
author_sort Malhotra, Ravinder Mohan
collection PubMed
description
format Online
Article
Text
id pubmed-5341278
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-53412782017-03-15 Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation Malhotra, Ravinder Mohan Al Mejally, Mousa Ali Abualela, Hanadi Mahmoud Eltemamy, Marwa Ahmed Ann Indian Acad Neurol Letters to the Editor Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5341278/ /pubmed/28298852 http://dx.doi.org/10.4103/0972-2327.194314 Text en Copyright: © 2006 - 2017 Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Letters to the Editor
Malhotra, Ravinder Mohan
Al Mejally, Mousa Ali
Abualela, Hanadi Mahmoud
Eltemamy, Marwa Ahmed
Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title_full Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title_fullStr Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title_full_unstemmed Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title_short Leber's hereditary optic neuropathy: Report of a simple case associated with a rare variant mutation
title_sort leber's hereditary optic neuropathy: report of a simple case associated with a rare variant mutation
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341278/
https://www.ncbi.nlm.nih.gov/pubmed/28298852
http://dx.doi.org/10.4103/0972-2327.194314
work_keys_str_mv AT malhotraravindermohan lebershereditaryopticneuropathyreportofasimplecaseassociatedwithararevariantmutation
AT almejallymousaali lebershereditaryopticneuropathyreportofasimplecaseassociatedwithararevariantmutation
AT abualelahanadimahmoud lebershereditaryopticneuropathyreportofasimplecaseassociatedwithararevariantmutation
AT eltemamymarwaahmed lebershereditaryopticneuropathyreportofasimplecaseassociatedwithararevariantmutation