Screening for Familial APP Mutations in Sporadic Cerebral Amyloid Angiopathy

BACKGROUND: Advances in genetic technology have revealed that variation in the same gene can cause both rare familial and common sporadic forms of the same disease. Cerebral amyloid angiopathy (CAA), a common cause of symptomatic intracerebral hemorrhage (ICH) in the elderly, can also occur in famil...

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Detalhes bibliográficos
Main Authors: Biffi, Alessandro, Plourde, Anna, Shen, Yiping, Onofrio, Robert, Smith, Eric E., Frosch, Matthew, Prada, Claudia M., Gusella, James, Greenberg, Steven M., Rosand, Jonathan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2010
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2978718/
https://ncbi.nlm.nih.gov/pubmed/21085603
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0013949
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