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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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| Publicado no: | Mol Neurobiol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer US
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8128844/ https://ncbi.nlm.nih.gov/pubmed/33464533 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-021-02282-4 |
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