Insulin-Independent and Dependent Glucose Transporters in Brain Mural Cells in CADASIL

Typical cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the human NOTCH3 gene. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy is characterized by subcortical ischemic strokes du...

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Detalles Bibliográficos
Autores principales: Panahi, Mahmod, Rodriguez, Patricia Rodriguez, Fereshtehnejad, Seyed-Mohammad, Arafa, Donia, Bogdanovic, Nenad, Winblad, Bengt, Cedazo-Minguez, Angel, Rinne, Juha, Darreh-Shori, Taher, Hase, Yoshiki, Kalaria, Raj N., Viitanen, Matti, Behbahani, Homira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522350/
https://www.ncbi.nlm.nih.gov/pubmed/33101365
http://dx.doi.org/10.3389/fgene.2020.01022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522350/
https://www.ncbi.nlm.nih.gov/pubmed/33101365
http://dx.doi.org/10.3389/fgene.2020.01022

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