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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Gepubliceerd in:Eur J Hum Genet
Hoofdauteurs: Mönkäre, Saana, Kuuluvainen, Liina, Kun-Rodrigues, Celia, Carmona, Susana, Schleutker, Johanna, Bras, Jose, Pöyhönen, Minna, Guerreiro, Rita, Myllykangas, Liisa
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer International Publishing 2020
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Article
Online toegang: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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