Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis

A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia

(2009) J. I. Arostegui et al.   BLOOD

Shwachman-Diamond syndrome neutrophils have altered chemoattractant-induced F-actin polymerization and polarization characteristics

(2009) C. Orelio et al.   HAEMATOLOGICA

Modulation of CXC Chemokine Receptor Expression and Function in Human Neutrophils during Aging In Vitro Suggests a Role in Their Clearance from Circulation

(2009) Katja C. Weisel et al.   MEDIATORS OF INFLAMMATION

The Many Causes of Severe Congenital Neutropenia

(2009) David C. Dale et al.   NEW ENGLAND JOURNAL OF MEDICINE

A Syndrome with Congenital Neutropenia and Mutations inG6PC3

(2009) Kaan Boztug et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genetic and molecular diagnosis of severe congenital neutropenia

(2008) Alister C Ward et al.   CURRENT OPINION IN HEMATOLOGY

Mitochondrial defects lie at the basis of neutropenia in Barth syndrome

(2008) Bram J van Raam et al.   CURRENT OPINION IN HEMATOLOGY