Rare diseases- Primary immunodeficiencies (PID)
- Defects of Vitamin B12 and Folate metabolism
- SLC46A1/PCFT deficiency causing hereditary folate malabsorbtion
European Reference Network for Immunodeficiency, Autoinflammatory, Autimmune and Pediatric Rheumatic disea
- Rare diseases
- Primary immunodeficiencies (PID)
- Defects of Vitamin B12 and Folate metabolism
- SLC46A1/PCFT deficiency causing hereditary folate malabsorbtion