The association between PQBP1 (Polyglutamine Binding Protein 1) and Renpenning Syndrome 1 is well established and manually curated, with its 4 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources4
Clinical variants49
Symptoms115
Compounds0
Trials0
Publications28
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.