Down-regulation of OPA1 in patients with primary open angle glaucoma

PURPOSE: Heterozygous optic atrophy type1 (OPA1) mutations are responsible for dominant optic atrophy, and the down regulation of OPA1 expression in patients with Leber hereditary optic neuropathy may imply that Opa1 protein levels in mitochondria play a role in other spontaneous optic neuropathies...

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Detalles Bibliográficos
Autores principales: Bosley, Thomas M., Hellani, Ali, Spaeth, George L., Myers, Jonathan, Katz, L. Jay, Moster, Marlene R., Milcarek, Barry, Abu-Amero, Khaled K.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086630/
https://www.ncbi.nlm.nih.gov/pubmed/21552501

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086630/
https://www.ncbi.nlm.nih.gov/pubmed/21552501

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