Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.

A1 Journal article (refereed)

Internal Authors/Editors

Publication Details

List of Authors: Hakonen AH, Goffart S, Marjavaara S, Paetau A, Cooper H, Mattila K, Lampinen M, Sajantila A, Lönnqvist T, Spelbrink JN, Suomalainen A.
Publication year: 2008
Journal: Human Molecular Genetics
Journal acronym: HMG
Volume number: 17
Issue number: 23
Start page: 3822
End page: 3835

Last updated on 2020-31-05 at 05:06