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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Detalles Bibliográficos
Autores principales: Biffi, Alessandro, Plourde, Anna, Shen, Yiping, Onofrio, Robert, Smith, Eric E., Frosch, Matthew, Prada, Claudia M., Gusella, James, Greenberg, Steven M., Rosand, Jonathan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978718/
https://www.ncbi.nlm.nih.gov/pubmed/21085603
http://dx.doi.org/10.1371/journal.pone.0013949

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978718/
https://www.ncbi.nlm.nih.gov/pubmed/21085603
http://dx.doi.org/10.1371/journal.pone.0013949

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