2. Academic Validation
  3. A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia

A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia

  • Blood. 2020 Jun 25;135(26):2427-2431. doi: 10.1182/blood.2019003178.
Michael Svaton 1,  Karolina Skvarova Kramarzova 1,  Veronika Kanderova 1,  Andrea Mancikova 2,  Petr Smisek 3,  Pavel Jesina 4,  Jakub Krijt 4,  Blanka Stiburkova 4 5,  Robert Dobrovolny 4,  Jitka Sokolova 4,  Violeta Bakardjieva-Mihaylova 1,  Elena Vodickova 6,  Marketa Rackova 1,  Jan Stuchly 1,  Tomas Kalina 1,  Jan Stary 3,  Jan Trka 1,  Eva Fronkova 1,  Viktor Kozich 4
Affiliations

Affiliations

  • 1 Childhood Leukemia Investigation Prague, Department of Pediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
  • 2 Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.
  • 3 Department of Pediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
  • 4 Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • 5 Institute of Rheumatology, Prague, Czech Republic; and.
  • 6 Department of Clinical Hematology, University Hospital Motol, Prague, Czech Republic.
PMID: 32276275 DOI: 10.1182/blood.2019003178
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