Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal. Issue 1 (9th December 2021)

Record Type:: Journal Article
Title:: Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal. Issue 1 (9th December 2021)
Main Title:: Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal
Authors:: Torraco, Alessandra
Maroofian, Reza
Rötig, Agnès
Bertini, Enrico
Ghezzi, Daniele
Carrozzo, Rosalba
Diodato, Daria
Abstract:
Is Part Of:: Human mutation. Volume 43:Issue 1(2022)
Journal:: Human mutation
Issue:: Volume 43:Issue 1(2022)
Issue Display:: Volume 43, Issue 1 (2022)
Year:: 2022
Volume:: 43
Issue:: 1
Issue Sort Value:: 2022-0043-0001-0000
Page Start:: 99
Page End:: 100
Publication Date:: 2021-12-09
Subjects:: Leigh syndrome -- mitochondrial disease -- NADH ubiquinone oxidoreductase -- NDUFA12
Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/humu.24303 ↗
Languages:: English
ISSNs:: 1059-7794
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 25792.xml