Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

Ítems similars

• Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia Registry
  per: Fioredda, Francesca, et al.
  Publicat: (2020)
• A zebrafish model for HAX1-associated congenital neutropenia
  per: Doll, Larissa, et al.
  Publicat: (2020)
• CSF3R MUTATIONS IN CONGENITAL NEUTROPENIA, A LONG STORY: DATA FROM THE ITALIAN REGISTRY
  per: Francesco Pegoraro, et al.
  Publicat: (2025-12-01)
• Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
  per: Tran, Tham Thi, et al.
  Publicat: (2018)
• Congenital pancreatic hypoplasia with neutropenia and skeletal abnormalities.
  per: McCollum, J. P., et al.
  Publicat: (1975)