ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins
Hum Mol Genet
.
2018 Oct 15;27(20):3650.
doi: 10.1093/hmg/ddy273.
Authors
Alessandra Torraco
1
,
Oliver Stehling
2
,
Claudia Stümpfig
2
,
Ralf Rösser
2
,
Domenico De Rasmo
3
,
Giuseppe Fiermonte
4
,
Daniela Verrigni
1
,
Teresa Rizza
1
,
Angelo Vozza
4
,
Michela Di Nottia
1
,
Daria Diodato
1
,
Diego Martinelli
5
,
Fiorella Piemonte
1
,
Carlo Dionisi-Vici
5
,
Enrico Bertini
1
,
Roland Lill
2
6
,
Rosalba Carrozzo
1
Affiliations
1
Laboratory of Molecular Medicine, Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
2
Institut für Zytobiologie, Philipps-Universität Marburg, Marburg, Germany.
3
Institute of Biomembrane, Bioenergetics and Molecular Biotechnology (IBIOM), National Research Council (CNR), Bari, Italy.
4
Laboratory of Biochemistry and Molecular Biology, Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.
5
Division of Metabolism, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
6
LOEWE Zentrum für Synthetische Mikrobiologie SynMikro, Marburg, Germany.
PMID:
30113620
DOI:
10.1093/hmg/ddy273
No abstract available