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
Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma.
Tateishi K et al.
Acta Neuropathologica Communications, 2023
38012788 (PubMed )
Supplement: 40478_2023_1683_MOESM2_ESM.xlsx › Supplementary_Table_S3
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