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Determination of Blood NOTCH3 Extracellular Domain and Jagged-1 Levels in Healthy Subjects
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common genetic disorder among those responsible for hereditary strokes, and it is caused by a mutation in the NOTCH3 gene on chromosome 19. Blood biomarkers related to the Notch signaling...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505916/ https://www.ncbi.nlm.nih.gov/pubmed/36142458 http://dx.doi.org/10.3390/ijms231810547 |