Minimal prevalence of Huntington’s disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions-Reference-Cited by-同舟云学术

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

Published:2019-06 Issue:2 Volume:42 Page:329-336
ISSN:1678-4685
Container-title:Genetics and Molecular Biology
language:
Short-container-title:Genet. Mol. Biol.

Author:

Castilhos Raphael Machado de¹,Santos José Augusto dos²,Augustin Marina Coutinho²,Pedroso José Luiz³,Barsottini Orlando³,Saba Roberta³,Ferraz Henrique Ballalai³,Godeiro Junior Clécio⁴,Vargas Fernando Regla⁵,Salarini Diego Zanotti⁶,Furtado Gabriel Vasata²,Polese-Bonatto Marcia²,Rodrigues Luiza Paulsen²,Sena Lucas Schenatto⁷,Saraiva-Pereira Maria Luiza⁸^ORCID,Jardim Laura Bannach⁹^ORCID

Affiliation:

1. Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Rede Neurogenética, Brazil; Instituto Nacional de Genética Médica Populacional (INAGEMP), Brazil

2. Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Rede Neurogenética, Brazil

3. Universidade Federal de São Paulo (UNIFESP), Brazil

4. Universidade Federal do Rio Grande do Norte (UFRN), Brazil

5. Universidade Federal do Estado do Rio de Janeiro (UNIRIO), Brazil; Instituto Oswaldo Cruz, Brazil

6. Santa Casa de Misericórdia de São Paulo, Brazil

7. Universidade Federal do Rio Grande do Sul (UFRGS), Brazil

8. Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Laboratório de Identificação Genética, Brazil; Serviço de Genética Médica, Brazil; Rede Neurogenética, Brazil

9. Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Universidade Federal do Rio Grande do Sul (UFRGS), Brazil; Laboratório de Identificação Genética, Brazil; Serviço de Genética Médica, Brazil; Rede Neurogenética, Brazil; Instituto Nacional de Genética Médica Populacional (INAGEMP), Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Link

http://www.scielo.br/pdf/gmb/v42n2/1415-4757-GMB-1678-4685-GMB-2018-0032.pdf

Reference27 articles.

1. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington’s disease;Andrew SE;Nat Genet,1993

2. Medical and social aspects of Huntington’s chorea in the state of Zulia, Venezuela;Ávila-Girón R;Adv Neurol,1973

3. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington’s disease;Aziz NA;Eur J Med Genet,2011

4. Huntington disease and Huntington disease-like in a case series from Brazil;Castilhos RM;Clin Genet,2014

5. Genetic aspects of Huntington’s disease in Latin America;Castilhos RM;A systematic review. Clin Genet,2016

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