Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations

INTRODUCTION: Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a relatively common cerebral small vessel disease. NOTCH3 has been identified as the causative gene of CADASIL. Clinical variability and genetic heterogeneity were observed in CADASI...

Descripción completa

Detalles Bibliográficos
Autores principales: Ni, Wang, Zhang, Yi, Zhang, Liang, Xie, Juan‐Juan, Li, Hong‐Fu, Wu, Zhi‐Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532899/
https://www.ncbi.nlm.nih.gov/pubmed/35822697
http://dx.doi.org/10.1111/cns.13917

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532899/
https://www.ncbi.nlm.nih.gov/pubmed/35822697
http://dx.doi.org/10.1111/cns.13917

Ejemplares similares