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A case of recurrent intracranial hemorrhage in CADASIL caused by NOTCH3 c.1759C>T heterozygous mutation
BACKGROUND: Cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a cerebrovascular disease that is closely related to the NOTCH3 gene. Recurrent ischemic stroke, progressive cognitive dysfunction, and mental symptoms are the main clinical manifestat...
Autores principales: | Chu, Ying, Wang, Qi, Ma, Yue, Xu, Linying, Ren, Kexin, Liu, Jiahui, Tao, Dingbo, Cao, Hua, Ji, Xiaofei |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937875/ https://www.ncbi.nlm.nih.gov/pubmed/36604800 http://dx.doi.org/10.1002/jcla.24840 |
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