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
De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes.
Loe-Mie Y et al.
Life (basel, Switzerland), 2024
38398753 (PubMed )
Supplement: life-14-00244-s001.zip › Supplementary_Table_2_SZ.xlsx › Feuil5
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