Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling

S Goffart, Helen Cooper, H Tyynismaa, S Wanrooij, A Suomalainen, JN Spelbrink

Research output: Contribution to journalArticleScientificpeer-review

88 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)328–340
JournalHuman Molecular Genetics
Issue number2
Publication statusPublished - 2009
MoE publication typeA1 Journal article-refereed

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