Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

01 aug 2010
Auteurs: Gerards M, Sluiter W van den Bosch BJC, de Wit LEA, Calis CMH, Frentzen M, Akbari H, Schoonderwoerd K, Scholte HR, Jongbloed RJ, Hendrickx ATM, de Coo IFM, Smeets HJM
Tijdschrift Journal of Medical Genetics
Impactfactor 5,751


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