The association between PRKAR1B (Protein Kinase CAMP-Dependent Type I Regulatory Subunit Beta) and Marbach-Schaaf Neurodevelopmental Syndrome 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 variants11
Symptoms56
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.