The association between SLC1A2 (Solute Carrier Family 1 Member 2) and Developmental And Epileptic Encephalopathy 41 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.
Sources4
Clinical variants46
Symptoms48
Compounds0
Trials0
Publications5
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.