PGAP1

PGAP1 deficiency, a GPI-anchor-related neurodevelopmental disorder

1 article(s) in the watch · Constitutional genetics

Curated publications

Expanding the genotypic and phenotypic spectrum of PGAP1 deficiency: clinical and functional insights from 15 patients.

PGAP1 deficiency, a GPI-anchor-related neurodevelopmental disorder

Automatic aggregation page — a clinical introduction may be added.