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

Author： Goffart Steffi   Cooper Helen M.   Tyynismaa Henna   Wanrooij Sjoerd   Suomalainen Anu   Spelbrink Johannes N.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.18, Iss.2, 2009-01, pp. : 328-340

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