NOTCH3 and CADASIL syndrome: a genetic and structural overview

CADASIL syndrome is a rare disease that belongs to a group of disorders called leukodystrophies. It is well established that NOTCH3 gene on chromosome 19 is primarily responsible for the development of the CADASIL syndrome. Herein, an attempt is made to shed light on the actual molecular mechanism u...

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Detalles Bibliográficos
Autores principales: Papakonstantinou, Eleni, Bacopoulou, Flora, Brouzas, Dimitrios, Megalooikonomou, Vasileios, D’Elia, Domenica, Bongcam-Rudloff, Erik, Vlachakis, Dimitrios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6583802/
https://www.ncbi.nlm.nih.gov/pubmed/31218211
http://dx.doi.org/10.14806/ej.24.0.921

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6583802/
https://www.ncbi.nlm.nih.gov/pubmed/31218211
http://dx.doi.org/10.14806/ej.24.0.921

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