ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins.
作者信息
Torraco Alessandra, Stehling Oliver, Stümpfig Claudia, Rösser Ralf, De Rasmo Domenico, Fiermonte Giuseppe, Verrigni Daniela, Rizza Teresa, Vozza Angelo, Di Nottia Michela, Diodato Daria, Martinelli Diego, Piemonte Fiorella, Dionisi-Vici Carlo, Bertini Enrico, Lill Roland, Carrozzo Rosalba
机构信息
Laboratory of Molecular Medicine, Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Institut für Zytobiologie, Philipps-Universität Marburg, Marburg, Germany.
出版信息
Hum Mol Genet. 2018 Oct 15;27(20):3650. doi: 10.1093/hmg/ddy273.
PMID:30113620
Abstract
摘要
Zotero 插件