F. Naso

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions

A. Durr, A. Brice, A. Novelletto, 1996, Annals of human genetics.

Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset

G. Colazza, F. Bianco, C. Morocutti, 2006, The Italian Journal of Neurological Sciences.

Nonisotopic method for accurate detection of (CAG)n repeats causing Huntington disease.

C. Grandinetti, F. Conforti, O. Leone, 1996, Clinical chemistry.

Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye‐of‐the‐tiger pattern

A. Quattrone, A. Gambardella, M. Zappia, 2006, Movement disorders : official journal of the Movement Disorder Society.