ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins. (2nd August 2018)

Record Type:: Journal Article
Title:: ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins. (2nd August 2018)
Main Title:: ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins
Authors:: 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
Abstract:
Is Part Of:: Human molecular genetics. Volume 27:Number 20(2018:Oct. 15)
Journal:: Human molecular genetics
Issue:: Volume 27:Number 20(2018:Oct. 15)
Issue Display:: Volume 27, Issue 20 (2018)
Year:: 2018
Volume:: 27
Issue:: 20
Issue Sort Value:: 2018-0027-0020-0000
Page Start:: 3650
Page End:: 3650
Publication Date:: 2018-08-02
Subjects:: Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8
Journal URLs:: http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗
DOI:: 10.1093/hmg/ddy273 ↗
Languages:: English
ISSNs:: 0964-6906
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 25180.xml