Selective Forces Related to Spinocerebellar Ataxia Type 2

A subcellular map of the human proteome

(2017) Peter J. Thul et al.   SCIENCE

Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions

(2016) G.N. Souza et al.   CLINICAL GENETICS

Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1

(2016) Fedor A. Platonov et al.   NEUROGENETICS

ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America

(2015) Fernanda S. Pereira et al.   CEREBELLUM

Spinocerebellar Ataxia Type 2: Clinical Presentation, Molecular Mechanisms, and Therapeutic Perspectives

(2012) J. J. Magaña et al.   MOLECULAR NEUROBIOLOGY

Infantile Childhood Onset of Spinocerebellar Ataxia Type 2

(2011) Roberto Di Fabio et al.   CEREBELLUM

Clinical utility gene card for: Usher syndrome

(2011) Hanno J Bolz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mechanisms of trinucleotide repeat instability during human development

(2010) Cynthia T. McMurray   NATURE REVIEWS GENETICS

Cellular and Molecular Pathways Triggering Neurodegeneration in the Spinocerebellar Ataxias

(2009) Antoni Matilla-Dueñas et al.   CEREBELLUM

Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy

(2008) A. Abdel-Aleem et al.   JOURNAL OF NEUROLOGY

Intrafamilial variability of Parkinson phenotype in SCAs: Novel cases due to SCA2 and SCA3 expansions

(2008) M.P. Socal et al.   PARKINSONISM & RELATED DISORDERS