Multi-system neurological disease is common in patients with OPA1 mutations

by Yu-, Griffiths, P. G., Gorman, G. S., Lourenco, C. M., Wright, A. F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M. L., Caporali, L., Lamperti, C., Tallaksen, C. M., Duffey, P., Miller, J., Whittaker, R. G., Baker, M. R., Jackson, M. J., Clarke, M. P., Dhillon, B., Czermin, B., Stewart, J. D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R .W, Turnbull, D. M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L .A, Horvath, R., Amati-Bonneau, P., Chinnery, P. F.
Published 2010