Loading...

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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Hovedforfatter: Bohlega, Saeed
Format: Artigo
Sprog:Inglês
Udgivet: PAGEPress Publications 2011
Fag:
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!