ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait

BACKGROUND: Leber's hereditary optic neuropathy (LHON) is a condition characterised by a rapid bilateral central vision loss due to death of the retinal ganglion cells, leading to visual impairment commonly occurring during young adulthood. The disease manifests itself more in male patients tha...

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Detalles Bibliográficos
Autores principales: Behbehani, Raed, Melhem, Motasem, Alghanim, Ghazi, Behbehani, Kazem, Alsmadi, Osama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Laboratory Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033154/
https://www.ncbi.nlm.nih.gov/pubmed/24568867
http://dx.doi.org/10.1136/bjophthalmol-2013-304140

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033154/
https://www.ncbi.nlm.nih.gov/pubmed/24568867
http://dx.doi.org/10.1136/bjophthalmol-2013-304140

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