The association between SLC31A1 (Solute Carrier Family 31 Member 1) and Neurodegeneration And Seizures Due To Copper Transport Defect is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.
Sources2
Clinical variants2
Symptoms47
Compounds0
Trials0
Publications2
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.