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Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose-6-phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm.

Authors
  • Krishnevskaya, Elena1
  • Rizzuto, Valeria1
  • Payán-Pernía, Salvador2, 3
  • Remacha, Ángel2, 3
  • Torrent, Montserrat2, 3
  • Ruiz, Anna4
  • Badell, Isabel2, 3, 5
  • Vives Corrons, Joan-Lluis1, 6
  • 1 Red Cell Pathology and Hematopoietic Disorders Unit (Rare Anaemias Expert Centre), Institute for Leukaemia Research Josep Carreras (IJC), Badalona (Barcelona), Spain. , (Spain)
  • 2 CSUR (Reference Centre) for Hereditary Red Cell Pathology, Hospital de la Santa Creu i Sant Pau, Universitat Autonoma de Barcelona, Barcelona, Spain. , (Spain)
  • 3 Institut de Recerca, Hospital de la Santa Creu i Sant Pau, Universitat Autonoma de Barcelona, Barcelona, Spain. , (Spain)
  • 4 Department d'Hematologia, Hospital de Sant Joan de Deu, Universitat Autònoma de Barcelona, Barcelona, Spain. , (Spain)
  • 5 Department de Pediatria, Hospital de la Santa Creu I Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain. , (Spain)
  • 6 Department de Medicina, Universitat de Barcelona, Barcelona, Spain. , (Spain)
Type
Published Article
Journal
International journal of laboratory hematology
Publication Date
Sep 20, 2019
Identifiers
DOI: 10.1111/ijlh.13110
PMID: 31539204
Source
Medline
Language
English
License
Unknown
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