Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

AIMS: Cerebral small vessel disease (SVD) is the leading cause of vascular dementia. Although the most of cases are sporadic, familial monogenic causes have been identified in a growing minority of patients. CADASIL, due to mutations of NOTCH3 gene, is the most common genetic SVD, and CARASIL, linke...

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Vydáno v:CNS Neurosci Ther
Hlavní autoři: Di Donato, Ilaria, Bianchi, Silvia, Gallus, Gian Nicola, Cerase, Alfonso, Taglia, Ilaria, Pescini, Francesca, Nannucci, Serena, Battisti, Carla, Inzitari, Domenico, Pantoni, Leonardo, Zini, Andrea, Federico, Antonio, Dotti, Maria Teresa
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2017
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6492684/
https://ncbi.nlm.nih.gov/pubmed/28782182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cns.12722
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