Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients

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 several dis...

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Bibliographic Details
Main Author: Rosa, A. (author)
Other Authors: Fonseca, B.V. (author), Krug, T. (author), Manso, H. (author), Gouveia, L. (author), Albergaria, I. (author), Gaspar, G. (author), Correia, M. (author), Viana-Baptista, M. (author), Simões, R.M. (author), Pinto, A.N. (author), Taipa, R. (author), Ferreira, C. (author), Fontes, J.R. (author), Silva, M.R. (author), Gabriel, J.P. (author), Matos, I. (author), Lopes, G. (author), Ferro, J.M. (author), Vicente, A.M. (author), Oliveira, S.A. (author)
Format: article
Language:eng
Published: 2011
Subjects:
Doenças Cardio e Cérebro-vasculares
Online Access:http://hdl.handle.net/10400.18/330
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/330

Internet

http://hdl.handle.net/10400.18/330

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