CDK5RAP3

Novel severe autosomal recessive neurodevelopmental syndrome linked to UFMylation

1 article(s) in the watch · Constitutional genetics

Curated publications

A severe neurodevelopmental syndrome linked to a South Asian founder variant in the UFMylation adaptor CDK5RAP3

Novel severe autosomal recessive neurodevelopmental syndrome linked to UFMylation

Automatic aggregation page — a clinical introduction may be added.