Blood Journal
Leading the way in experimental and clinical research in hematology

The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy

  1. Polina Stepensky1,
  2. Ann Saada2,
  3. Marianne Cowan3,
  4. Adi Tabib4,
  5. Ute Fischer5,
  6. Yackov Berkun6,
  7. Hani Saleh7,
  8. Natalia Simanovsky8,
  9. Aviram Kogot-Levin2,
  10. Michael Weintraub1,
  11. Hamam Ganaiem6,
  12. Avraham Shaag2,
  13. Shamir Zenvirt2,
  14. Arndt Borkhardt5,
  15. Orly Elpeleg2,
  16. Nia J. Bryant3, and
  17. Dror Mevorach4
  1. 1Department of Pediatric Hematology-Oncology, and
  2. 2Monique and Jacques Roboh Department of Genetic Research, Hadassah, Hebrew University Medical Center, Jerusalem, Israel;
  3. 3Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom;
  4. 4Rheumatology Research Center and Department of Medicine, Hadassah, Hebrew University Medical Center, Jerusalem, Israel;
  5. 5Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Center of Child and Adolescent Health, Heinrich Heine University, Düsseldorf, Germany;
  6. 6Department of Pediatrics, Hadassah-Hebrew University Medical Center, Jerusalem, Israel;
  7. 7Pediatric Hemato-Oncology Unit, Augusta Victoria Hospital, Jerusalem; and
  8. 8Department of Radiology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
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