First Case of X-Linked Moesin Deficiency Identified After Newborn Screening for SCID

Ítems similars

• Two Unique Cases of X-linked SCID: A Diagnostic Challenge in the Era of Newborn Screening
  per: Purswani, Pooja, et al.
  Publicat: (2019)
• Immune dysregulation in patients with RAG deficiency and other forms of combined immune deficiency
  per: Delmonte, Ottavia M., et al.
  Publicat: (2020)
• RAG Deficiency: Two Genes, Many Diseases
  per: Delmonte, Ottavia M., et al.
  Publicat: (2018)
• Complete Absence of CD3γ Protein Expression Is Responsible for Combined Immunodeficiency with Autoimmunity Rather than SCID
  per: Delmonte, Ottavia M., et al.
  Publicat: (2020)
• Progressive B-cell loss in revertant X-SCID
  per: Lin, Connie H., et al.
  Publicat: (2020)