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Association of a Genetic Variant in the <i>ALOX5AP</i> with Higher Risk of Ischemic Stroke: A Case-Control, Meta-Analysis and Functional Study
Author(s) -
Sophie DominguesMontanari,
Israel FernándezCadenas,
Alberto del Río-Espínola,
Natália Corbeto,
Tiago Krug,
Helena Manso,
Liliana Gouveia,
João Sobral,
Maite Mendióroz,
Jessica FernándezMorales,
José ÁlvarezSabín,
Marc Ribó,
Marta Rubiera,
Vı́ctor Obach,
Joan MartíFàbregas,
Marimar Freijó,
Joaquı́n Serena,
José M. Ferro,
Astrid M. Vicente,
Sofia A. Oliveira,
Joan Montaner
Publication year - 2010
Publication title -
cerebrovascular diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.221
H-Index - 104
eISSN - 1421-9786
pISSN - 1015-9770
DOI - 10.1159/000302738
Subject(s) - single nucleotide polymorphism , medicine , snp , genetic association , genome wide association study , genetics , allele , gene , genotype , biology
Variants in the 5-lipoxygenase-activating protein (ALOX5AP) and phosphodiesterase 4D (PDE4D) genes have first been associated with ischemic stroke (IS) through whole-genome linkage screens. However, association studies obtained conflicting results. We aimed to investigate the contribution of selected single nucleotide polymorphisms (SNPs) in these genes for the first time in a large Iberian population.

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