Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Rare Variant Association Analysis Uncovers Involvement of VNN2 in Stroke Outcome.
Alcaide-Consuegra E et al.
Stroke, 2025
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