Whole-exome sequencing of Finnish patients with vascular cognitive impairment

Cerebral small vessel disease (CSVD) is the most important cause of vascular cognitive impairment (VCI). Most CSVD cases are sporadic but familial monogenic forms of the disorder have also been described. Despite the variants identified, many CSVD cases remain unexplained genetically. We used whole-...

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Bibliographic Details
Published in:Eur J Hum Genet
Main Authors: Mönkäre, Saana, Kuuluvainen, Liina, Kun-Rodrigues, Celia, Carmona, Susana, Schleutker, Johanna, Bras, Jose, Pöyhönen, Minna, Guerreiro, Rita, Myllykangas, Liisa
Format: Artigo
Language:Inglês
Published: Springer International Publishing 2020
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC8115269/
https://ncbi.nlm.nih.gov/pubmed/33268848
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-00775-9
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