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

Ngā tūemi rite

• Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
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• A zebrafish model for HAX1-associated congenital neutropenia
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• Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia
  mā: Marina Lanciotti, me ētahi atu.
  I whakaputaina: (2010-01-01)
• Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency
  mā: K. Matsubara, me ētahi atu.
  I whakaputaina: (2007-12-01)
• P779: LONG-TERM COURSE OF HAX1-RELATED CONGENITAL NEUTROPENIA: AN ANALYSIS OF THE EUROPEAN SEVERE CHRONIC NEUTROPENIA INTERNATIONAL REGISTRY (SCNIR)
  mā: Denys Pogozhykh, me ētahi atu.
  I whakaputaina: (2023-08-01)