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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...

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Foilsithe in:BMJ Case Rep
Main Authors: Dunphy, Louise, Rani, Amir, Duodu, Yaw, Behnam, Yousef
Formáid: Artigo
Teanga:Inglês
Foilsithe: BMJ Publishing Group 2019
Ábhair:
Rochtain Ar Líne: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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