COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage

OBJECTIVE: Mutations in the type IV collagen alpha 1 gene (COL4A1) cause dominantly inherited cerebrovascular disease. We seek to determine the extent to which COL4A1 mutations contribute to sporadic, non-familial, intracerebral hemorrhages (ICHs). METHODS: We sequenced COL4A1 in 96 patients with sp...

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Detalhes bibliográficos
Main Authors: Weng, Yi-Chinn, Sonni, Akshata, Labelle-Dumais, Cassandre, de Leau, Michelle, Kauffman, W. Berkeley, Jeanne, Marion, Biffi, Alessandro, Greenberg, Steven M., Rosand, Jonathan, Gould, Douglas B.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3335762/
https://ncbi.nlm.nih.gov/pubmed/22522439
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.22682
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