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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) presenting with stroke in a young man

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene which maps to the short arm of chromosome 19 and encodes the NOTCH3 receptor protein, predominantly expressed in adults by vascular smooth muscle cells and p...

詳細記述

保存先:
書誌詳細
出版年:BMJ Case Rep
主要な著者: Dunphy, Louise, Rani, Amir, Duodu, Yaw, Behnam, Yousef
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Publishing Group 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6663233/
https://ncbi.nlm.nih.gov/pubmed/31324668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-229609
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