Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.

Leber's hereditary optic neuropathy (LHON) is a maternally transmitted disease causing acute or subacute, bilateral optic atrophy mainly in young men. It is found to be a mitochondrial disorder with the primary mitochondrial DNA (mtDNA) mutations at 11,778, 3460, and 14,484. The incidence of ea...

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Detalles Bibliográficos
Autores principales: Hwang, Jeong-Min, Chang, Bong Leen, Koh, Hyoung Jun, Kim, Ji Yeon, Park, Sung Sup
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2002
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054852/
https://www.ncbi.nlm.nih.gov/pubmed/11961321

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054852/
https://www.ncbi.nlm.nih.gov/pubmed/11961321

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