P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance

✍ Scribed by Gorman, G.S.; Pfeffer, G.; Griffin, H.; Kurzawa-Akanbi, M.; Blakely, E.L.; Wilson, I.; Sitarz, K.; Moore, D.; Murphy, J.L.; Alston, C.L.; Pyle, A.; Coxhead, J.; Payne, B.; Gorrie, G.H.; Longman, C.; Hadjivassiliou, M.; McConville, J.; Dick, D.; Imam, I.; Hilton, D.; Norwood, F.; Baker, M.R.; Jaiser, S.R.; Yu-Wai-Man, P.; Farrell, M.; McCarthy, A.; Lynch, T.; McFarland, R.; Schaefer, A.M.; Turnbull, D.M.; Horvath, R.; Taylor, R.W.; Chinnery, P.F.

• Book ID: 122161710
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 56 KB
• Volume: 24
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/S0960-8966(14)70048-3