Associated Papers
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations.
Liu D et al.
Nature Genetics, 2023
36914870 (PubMed )
Supplement: 41588_2023_1305_MOESM4_ESM.xlsx › Supplementary_Table_8
Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.
Ehtesham N et al.
Archives of Iranian Medicine, 2022
37543906 (PubMed )
Supplement: aim-25-788-s002.xlsx › Table_S1.7
Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy.
Berecki G et al.
International Journal of Molecular Sciences, 2020
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania.
Ware TL et al.
Epilepsia Open, 2019
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