Sandra T. Cooper

1. A severe neurodevelopmental syndrome linked to a South Asian founder variant in the UFMylation adaptor CDK5RAP3
   2026/04/27 by Michaela Yuen, Katharine Zhang, Rhett G. Marchant +23 · 1 voice
   Biochemistry, Genetics and Molecular Biology · #Connective tissue disorders research #Genetics and Neurodevelopmental Disorders #Genomics and Rare Diseases