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pro vyhledávání: '"N. Pérez-Bravo"'
Autor:
J. Macuada, I. Molina-Riquelme, G. Vidal, N. Pérez-Bravo, C. Vásquez-Trincado, G. Aedo, D. Lagos, P. Yu-Wai-Man, R. Horvath, T. J. Rudge, B. Cartes-Saavedra, V. Eisner
Publikováno v:
Cell Death and Disease, Vol 15, Iss 11, Pp 1-10 (2024)
Abstract Optic atrophy protein 1 (OPA1) mediates inner mitochondrial membrane (IMM) fusion and cristae organization. Mutations in OPA1 cause autosomal dominant optic atrophy (ADOA), a leading cause of blindness. Cells from ADOA patients show impaired
Externí odkaz:
https://doaj.org/article/fde6a90279e94de0badf99ed7309880a
