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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Detalles Bibliográficos
Autores principales: Kumar, Manoj, Tanwar, Mukesh, Saxena, Rohit, Sharma, Pradeep, Dada, Rima
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862244/
https://www.ncbi.nlm.nih.gov/pubmed/20454697

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862244/
https://www.ncbi.nlm.nih.gov/pubmed/20454697

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