Novel mutation of the notch3 gene in arabic family with CADASIL

Mutations in the NOTCH3 gene are responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), an adult onset hereditary angiopathy leading to ischemic stroke, vascular dementia and psychiatric disorders. All mutation of NOTCH3 described so far...

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Detalles Bibliográficos
Autor principal: Bohlega, Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207232/
https://www.ncbi.nlm.nih.gov/pubmed/22053260
http://dx.doi.org/10.4081/ni.2011.e6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207232/
https://www.ncbi.nlm.nih.gov/pubmed/22053260
http://dx.doi.org/10.4081/ni.2011.e6

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