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Identification of novel mitochondrial mutations in Leber’s hereditary optic neuropathy

PURPOSE: To screen mitochondrial DNA (mtDNA) variations in Leber hereditary optic neuropathy (LHON). METHODS: Ten LHON patients were selected from neuro-ophthalmology clinics of All India Institute of Medical Sciences (AIIMS), New Delhi, India. Clinical evaluation included slit-lamp biomicroscopy, f...

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Detalhes bibliográficos
Main Authors: Kumar, Manoj, Tanwar, Mukesh, Saxena, Rohit, Sharma, Pradeep, Dada, Rima
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2862244/
https://ncbi.nlm.nih.gov/pubmed/20454697
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