Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series

Por van de Leemput, J, Wavrant-De Vrièze, F, Rafferty, I, Bras, JM, Giunti, P, Fisher, EMC, Hardy, J, Singleton, AB, Houlden, H
Publicado em 2010

Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19

Por Meilleur, K.G., Traoré, M., Sangaré, M., Britton, A., Landouré, G., Coulibaly, S., Niaré, B., Mochel, F., La Pean, A., Rafferty, I., Watts, C., Littleton-Kearney, M. T., Blackstone, C., Singleton, A., Fischbeck, K.H.
Publicado em 2009