Contribution of “Omic” Studies to the Understanding of Cadasil. A Systematic Review

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a small vessel disease caused by mutations in NOTCH3 that lead to an odd number of cysteines in the epidermal growth factor (EGF)-like repeat domain, causing protein misfolding and aggregation. Th...

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Detalles Bibliográficos
Autores principales: Muiño, Elena, Fernández-Cadenas, Israel, Arboix, Adrià
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304933/
https://www.ncbi.nlm.nih.gov/pubmed/34298974
http://dx.doi.org/10.3390/ijms22147357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304933/
https://www.ncbi.nlm.nih.gov/pubmed/34298974
http://dx.doi.org/10.3390/ijms22147357

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