P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance
Titel:
P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance
Auteur:
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.