Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders-Reference-Cited by-同舟云学术

Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

Published:2016-09 Issue: Volume:30 Page:51-58
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Yubero Delia,Montero Raquel,Martín Miguel A.,Montoya Julio,Ribes Antonia,Grazina Manuela,Trevisson Eva,Rodriguez-Aguilera Juan Carlos,Hargreaves Iain P.,Salviati Leonardo,Navas Plácido,Artuch Rafael,Jou Cristina,Jimenez-Mallebrera Cecilia,Nascimento Andres,Pérez-Dueñas Belén,Ortez Carlos,Ramos Federico,Colomer Jaume,O’Callaghan Mar,Pineda Mercè,García-Cazorla Angels,Espinós Carmina,Ruiz Angels,Macaya Alfons,Marcé-Grau Anna,Garcia-Villoria Judit,Arias Angela,Emperador Sonia,Ruiz-Pesini Eduardo,Lopez-Gallardo Ester,Neergheen Viruna,Simões Marta,Diogo Luisa,Blázquez Alberto,González-Quintana Adrián,Delmiro Aitor,Domínguez-González Cristina,Arenas Joaquín,García-Silva Mª Teresa,Martín Elena,Quijada Pilar,Hernández-Laín Aurelio,Morán María,Rivas Infante Eloy,Ávila Polo Rainiero,Paradas Lópe Carmen,Bautista Lorite Juan,Martínez Fernández Eva M.,Cortés Ana B.,Sánchez-Cuesta Ana,Cascajo Maria V.,Alcázar María,Brea-Calvo Gloria

Funder

Instituto de Salud Carlos III

Explora Ciencia Program

Universidad del Gobierno de Aragón

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

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3. Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q10 content;Asencio;Eur. J. Hum. Genet.,2016