Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins.AuthorsTorraco, Alessandra; Stehling, Oliver; Stümpfig, Claudia; Rösser, Ralf; Rasmo, Domenico De; Fiermonte, Giuseppe; Verrigni, Daniela; Rizza, Teresa; Vozza, Angelo; Nottia, Michela DiPublicationHuman Molecular Genetics, 2018, Vol 27, Issue 20, p3650ISSN0964-6906Publication typeArticleDOI10.1093/hmg/ddy273