Genetic study of the NOTCH3 gene in CADASIL patients
Background: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a monogenic, hereditary, neurological syndrome characterized by small vessel disease (SVD), stroke, vascular cognitive impairment and dementia. It is caused by mutations in the NOTCH3...
Na minha lista:
| Principais autores: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SpringerOpen
2018-10-01
|
| coleção: | Egyptian Journal of Medical Human Genetics |
| Acesso em linha: | http://www.sciencedirect.com/science/article/pii/S1110863018300624 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|