CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a monogenic disease caused by NOTCH3 mutations and characterized by typical clinical, neuroradiological, and pathological features. NOTCH3 belongs to a family of highly conserved transmembrane rec...

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Detalles Bibliográficos
Autores principales: Manini, Arianna, Pantoni, Leonardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128844/
https://www.ncbi.nlm.nih.gov/pubmed/33464533
http://dx.doi.org/10.1007/s12035-021-02282-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128844/
https://www.ncbi.nlm.nih.gov/pubmed/33464533
http://dx.doi.org/10.1007/s12035-021-02282-4

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