APA

Crimella C., Arnoldi A., Crippa F., Mostacciuolo M. L., Boaretto F., Sironi M., D'Angelo M. G., Manzoni S., Piccinini L., Turconi A. C., Toscano A., Musumeci O., Benedetti S., Fazio R., Bresolin N., Daga A., Martinuzzi A. & Bassi M. T. (20090925). Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. : Journal of medical genetics.

Chicago

Crimella C, Arnoldi A, Crippa F, Mostacciuolo M L, Boaretto F, Sironi M, D'Angelo M Grazia, Manzoni S, Piccinini L, Turconi A C, Toscano A, Musumeci O, Benedetti S, Fazio R, Bresolin N, Daga A, Martinuzzi A and Bassi M T. 20090925. Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. : Journal of medical genetics.

Harvard

Crimella C., Arnoldi A., Crippa F., Mostacciuolo M. L., Boaretto F., Sironi M., D'Angelo M. G., Manzoni S., Piccinini L., Turconi A. C., Toscano A., Musumeci O., Benedetti S., Fazio R., Bresolin N., Daga A., Martinuzzi A. and Bassi M. T. (20090925). Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. : Journal of medical genetics.

MLA

Crimella C, Arnoldi A, Crippa F, Mostacciuolo M L, Boaretto F, Sironi M, D'Angelo M Grazia, Manzoni S, Piccinini L, Turconi A C, Toscano A, Musumeci O, Benedetti S, Fazio R, Bresolin N, Daga A, Martinuzzi A and Bassi M T. Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. : Journal of medical genetics. 20090925.