Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Morgane LeMao"'
Autor:
Majida, Charif, Naïg, Gueguen, Marc, Ferré, Zouhair, Elkarhat, Salim, Khiati, Morgane, LeMao, Arnaud, Chevrollier, Valerie, Desquiret-Dumas, David, Goudenège, Céline, Bris, Selma, Kane, Jennifer, Alban, Stéphanie, Chupin, Céline, Wetterwald, Leonardo, Caporali, Francesca, Tagliavini, Chiara, LaMorgia, Michele, Carbonelli, Neringa, Jurkute, Abdelhamid, Barakat, Philippe, Gohier, Christophe, Verny, Magalie, Barth, Vincent, Procaccio, Dominique, Bonneau, Xavier, Zanlonghi, Isabelle, Meunier, Nicole, Weisschuh, Simone, Schimpf-Linzenbold, Felix, Tonagel, Ulrich, Kellner, Patrick, Yu-Wai-Man, Valerio, Carelli, Bernd, Wissinger, Patrizia, Amati-Bonneau, Pascal, Reynier, Guy, Lenaers
Publikováno v:
Brain Communications
Biallelic mutations in ACO2, encoding the mitochondrial aconitase 2, have been identified in individuals with neurodegenerative syndromes, including infantile cerebellar retinal degeneration and recessive optic neuropathies (locus OPA9). By screening
Autor:
Chiara LaMorgia, Pascal Reynier, Céline Wetterwald, Vincent Procaccio, Simone Schimpf-Linzenbold, Bernd Wissinger, Valérie Desquiret-Dumas, Stéphanie Chupin, Felix Tonagel, Leonardo Caporali, Selma Kane, Valerio Carelli, Magalie Barth, Naïg Gueguen, Xavier Zanlonghi, Majida Charif, Patrick Yu-Wai-Man, Neringa Jurkute, Morgane LeMao, Francesca Tagliavini, David Goudenège, Zouhair Elkarhat, Céline Bris, Marc Ferré, Jennifer Alban, Isabelle Meunier, Guy Lenaers, Arnaud Chevrollier, Abdelhamid Barakat, Ulrich Kellner, Patrizia Amati-Bonneau, Christophe Verny, Salim Khiati, Nicole Weisschuh, Philippe Gohier, Michele Carbonelli, Dominique Bonneau
Publikováno v:
Brain Communications
Brain Communications, 2021, 3 (2), ⟨10.1093/braincomms/fcab063⟩
Brain Communications, 2021, 3 (2), ⟨10.1093/braincomms/fcab063⟩
Biallelic mutations in ACO2, encoding the mitochondrial aconitase 2, have been identified in individuals with neurodegenerative syndromes, including infantile cerebellar retinal degeneration and recessive optic neuropathies (locus OPA9). By screening