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

S Goffart; H Cooper; H Tyynismaa; S Wanrooij; A Suomalainen; J Spelbrink

doi:10.1093/hmg/ddn359

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

S Goffart
, H Cooper
, H Tyynismaa
, S Wanrooij
, A Suomalainen
, J Spelbrink

Department of Clinical Chemistry

Research output: Contribution to journal › Article › Scientific › peer-review

127 Citations (Scopus)

Original language	English
Pages (from-to)	328-340
Journal	Human Molecular Genetics
Volume	18
Issue number	2
DOIs	https://doi.org/10.1093/hmg/ddn359
Publication status	Published - 2009
Publication type	A1 Journal article-refereed

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10.1093/hmg/ddn359

Cite this

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

author = "S Goffart and H Cooper and H Tyynismaa and S Wanrooij and A Suomalainen and J Spelbrink",

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AU - Goffart, S

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AU - Wanrooij, S

AU - Suomalainen, A

AU - Spelbrink, J

PY - 2009

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DO - 10.1093/hmg/ddn359

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SN - 0964-6906

VL - 18

SP - 328

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JO - Human Molecular Genetics

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IS - 2

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