https://orcid.org/0000-0001-9276-4590
-
PDF
- Split View
-
Views
-
Cite
Cite
Alessandra Torraco, Oliver Stehling, Claudia Stümpfig, Ralf Rösser, Domenico De Rasmo, Giuseppe Fiermonte, Daniela Verrigni, Teresa Rizza, Angelo Vozza, Michela Di Nottia, Daria Diodato, Diego Martinelli, Fiorella Piemonte, Carlo Dionisi-Vici, Enrico Bertini, Roland Lill, Rosalba Carrozzo, ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins, Human Molecular Genetics, Volume 27, Issue 20, 15 October 2018, Page 3650, https://doi.org/10.1093/hmg/ddy273
Close - Share Icon Share
Human Molecular Genetics, 2018, 27(15), 2739–2754.
doi: 10.1093/hmg/ddy183.
This article initially published with the incorrect supplementary material. This error has now been corrected, and the correct supplementary material is published.
The publisher regrets the error.
Author notes
Alessandra Torraco and Oliver Stehling authors contributed equally to this work.
Enrico Bertini, Roland Lill and Rosalba Carrozzo authors contributed equally as senior authors.
