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Article

Genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro, Brazil.

Arquivos de neuro-psiquiatria - 1 Jun 2011

Filho Isaac Lima da Silva, Leite Ana Claudia Celestino Bezerra, Moura Patrícia Gomes, Ribeiro Georgina Severo, Cavalcante Andréa Cony, Azevedo Flávia Carolina Marques de, Andrada-Serpa Maria José de

Abstract excerpt

The aim of the present work was to examine possible genetic risk factors related to the occurrence of cerebrovascular disease (CVD) in Brazilian population, the frequency of β(S)-globin gene haplotypes and co-inheritance with α-thalassemia (-α(3.7kb)) and single nucleotide polymorphism of methylenetetrahydrofolate reductase (MTHFR-C677T), Factor V Leiden (FV-G1691A) and prothrombin (PT-G20210A) genes in children...

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Identifiers

PMID: 21755116
DOI: 10.1590/s0004-282x2011000400004

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MTHFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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