Minimal prevalence of Huntington’s disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions

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

The Prevalence of Huntington's Disease

(2016) Michael D. Rawlins et al.   NEUROEPIDEMIOLOGY

Genetic aspects of Huntington's disease in Latin America. A systematic review

(2015) R.M. Castilhos et al.   CLINICAL GENETICS

High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population

(2013) Alicia Semaka et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Huntington disease and Huntington disease-like in a case series from Brazil

(2013) R.M. Castilhos et al.   CLINICAL GENETICS

Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington’s disease

(2011) N. Ahmad Aziz et al.   European Journal of Medical Genetics

Intergenerational instability in Huntington disease: Extreme repeat changes among 134 transmissions

(2011) Eliana Marisa Ramos et al.   MOVEMENT DISORDERS

Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population

(2010) J Sequeiros et al.   CLINICAL GENETICS

Geographic Patterns of Genome Admixture in Latin American Mestizos

(2008) Sijia Wang et al.   PLoS Genetics