ロード中...

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...

詳細記述

保存先:
書誌詳細
第一著者: Bohlega, Saeed
フォーマット: Artigo
言語:Inglês
出版事項: PAGEPress Publications 2011
主題:
オンライン・アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!