OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Autor: Rafael Garesse, Carmen Ayuso, Bernd Wissinger, Katell Beauvais, Luisa Iommarini, Joaquiotan Arenas, Dominique Figarella-Branger, Yolanda Campos, Valerio Carelli, Chiara La Morgia, Miguel A. Martín, Alain Furby, Michela Rugolo, Andrea Cossarizza, Claudia Zanna, Pascal Reynier, Pascale Marcorelles, Maria Liguori, Henry Rivera, Jesús González de la Aleja, Pasquale Montagna, María Esther Gallardo, Guy Lenaers, Robert Schwarzenbacher, Rosanna Carroccia, Patrizia Amati-Bonneau, Franck Letournel, Dominique Bonneau, Rocco Liguori, Belén Bornstein, Anne Boissiere, Maria Lucia Valentino, Christophe Verny, Pierre Labauge

Publikováno v: Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Brain-A Journal of Neurology, 2008, 131 (Pt 2), pp.338-51. ⟨10.1093/brain/awm298⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License.-- et al.
Mutations in OPA1, a dynamin-related GTPase involved in mitochondrial fusion, cristae organization and control of apo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeca1b2b92e1571ea516c89c32dd04b4
https://www.hal.inserm.fr/inserm-00293604