Associated Papers
Rare Variant Association Analysis Uncovers Involvement of VNN2 in Stroke Outcome.
Alcaide-Consuegra E et al.
Stroke, 2025
Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.
Fidalgo F et al.
Plos One, 2022
35085295 (PubMed )
Supplement: pone.0262419.s002.xlsx › 288_candidate_variants
Select a paper to view details