Associated Papers
A Novel APP p.V742L variant in a patient with ischemic small vessel disease enhances FE65 signalling.
Voesenek BJB et al.
Neurobiology of Disease, 2026
Building a hereditary cancer program in Colombia: analysis of germline pathogenic and likely pathogenic variants spectrum in a high-risk cohort.
Sanabria-Salas MC et al.
European Journal of Human Genetics : Ejhg, 2025
The role of multi-organ cancer predisposition genes in the risk of inherited and histologically diverse gastric cancer.
Guerra J et al.
Ebiomedicine, 2025
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