Screening of Twinkle gene in POLG1- and ANT1-negative patients with mitochondrial myopathy and multiple mitochondrial DNA deletions: four new mutations
dc.creator | Virgilio, R. | en |
dc.creator | Ronchi, D. | en |
dc.creator | Bordoni, A. | en |
dc.creator | Adobbati, L. | en |
dc.creator | Hadjigeorgiou, G. M. | en |
dc.creator | Kafet-Souli, D. | en |
dc.creator | Tsironi, E. | en |
dc.creator | Papadimitriou, A. | en |
dc.creator | Moggio, M. | en |
dc.creator | Bresolin, N. | en |
dc.creator | Comi, G. P. | en |
dc.date.accessioned | 2015-11-23T10:53:41Z | |
dc.date.available | 2015-11-23T10:53:41Z | |
dc.date.issued | 2006 | |
dc.identifier.issn | 0340-5354 | |
dc.identifier.uri | http://hdl.handle.net/11615/34489 | |
dc.source.uri | <Go to ISI>://WOS:000238478600135 | |
dc.subject | Clinical Neurology | en |
dc.title | Screening of Twinkle gene in POLG1- and ANT1-negative patients with mitochondrial myopathy and multiple mitochondrial DNA deletions: four new mutations | en |
dc.type | journalArticle | en |
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