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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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書目詳細資料
主要作者: Bohlega, Saeed
格式: Artigo
語言:Inglês
出版: PAGEPress Publications 2011
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3207232/
https://ncbi.nlm.nih.gov/pubmed/22053260
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/ni.2011.e6
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