Author:
Ait-El-Mkadem Samira,Dayem-Quere Manal,Gusic Mirjana,Chaussenot Annabelle,Bannwarth Sylvie,François Bérengère,Genin Emmanuelle C.,Fragaki Konstantina,Volker-Touw Catharina L.M.,Vasnier Christelle,Serre Valérie,van Gassen Koen L.I.,Lespinasse Françoise,Richter Susan,Eisenhofer Graeme,Rouzier Cécile,Mochel Fanny,De Saint-Martin Anne,Abi Warde Marie-Thérèse,de Sain-van der Velde Monique G.M.,Jans Judith J.M.,Amiel Jeanne,Avsec Ziga,Mertes Christian,Haack Tobias B.,Strom Tim,Meitinger Thomas,Bonnen Penelope E.,Taylor Robert W.,Gagneur Julien,van Hasselt Peter M.,Rötig Agnès,Delahodde Agnès,Prokisch Holger,Fuchs Sabine A.,Paquis-Flucklinger Véronique
Funder
Fondation pour la Recherche Médicale
Fondation Maladies Rares
German Bundesministerium für Bildung und Forschung (BMBF) through the E-Rare project GENOMIT
BMBF through the Juniorverbund in der Systemmedizin “mitOmics”
EU FP7 Mitochondrial European Educational Training Project
EU Horizon2020 Collaborative Research Project SOUND
Wellcome Trust Strategic Award
Medical Research Council Centre for Neuromuscular Diseases
Lily Foundation
UK National Health Service Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service
NIH National Institute of Neurological Disorders and Stroke
Subject
Genetics(clinical),Genetics
Cited by
70 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献