ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins.
Torraco A, Stehling O, Stümpfig C, Rösser R, De Rasmo D, Fiermonte G, Verrigni D, Rizza T, Vozza A, Di Nottia M, Diodato D, Martinelli D, Piemonte F, Dionisi-Vici C, Bertini E, Lill R, Carrozzo R.
Torraco A, et al. Among authors: rosser r.
Hum Mol Genet. 2018 Oct 15;27(20):3650. doi: 10.1093/hmg/ddy273.
Hum Mol Genet. 2018.
PMID: 30113620
No abstract available.