Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patient

BACKGROUND: The genetic contribution to stroke is well established but it has proven difficult to identify the genes and the disease-associated alleles mediating this effect, possibly because only nuclear genes have been intensely investigated so far. Mitochondrial DNA (mtDNA) has been implicated in...

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Detalhes bibliográficos
Autor principal: Rosa, A (author)
Outros Autores: Fonseca, BV (author), Krug, T (author), Manso, H (author), Gouveia, L (author), Albergaria, I (author), Gaspar, G (author), Correia, M (author), Viana-Baptista, M (author), Simões, RM (author), Pinto, AN (author), Taipa, R (author), Ferreira, C (author), Fontes, JR (author), Gabriel, JP (author), Matos, I (author), Lopes, G (author), Ferro, JM (author), Vicente, AM (author), Oliveira, SA (author)
Formato: article
Idioma:eng
Publicado em: 2012
Assuntos:
Isquemia Cerebral
DNA Mitocondrial
Predisposição Genética para Doença
Haplótipos
Acidente Vascular Cerebral
Texto completo:http://hdl.handle.net/10400.23/300
País:Portugal
Oai:oai:repositorio.hospitaldebraga.pt:10400.23/300

Texto Completo

http://hdl.handle.net/10400.23/300

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