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

AH Hakonen, S Goffart, S Marjavaara, A Paetau, Helen Cooper, K Mattila, M Lampinen, A Sajantila, T Lönnqvist, JN Spelbrink, A. Suomalainen

Research output: Contribution to journalArticleScientificpeer-review

119 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)3822–3835
JournalHuman Molecular Genetics
Issue number23
Publication statusPublished - 2008
MoE publication typeA1 Journal article-refereed

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