CADASIL in Arabs: clinical and genetic findings

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is increasingly recognized as an inherited arterial disease leading to a step-wise decline and eventually to dementia. CADASIL is caused by mutations in NOTCH3 epidermal growth factor-lik...

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Detalhes bibliográficos
Main Authors: Bohlega, Saeed, Al Shubili, Asmahan, Edris, Abdulrahman, Alreshaid, Abdulrahman, AlKhairallah, Thamer, AlSous, M Walid, Farah, Samir, Abu-Amero, Khaled K
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2007
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2190758/
https://ncbi.nlm.nih.gov/pubmed/17996090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-67
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