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Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose‐6‐phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm
Author(s) -
Krishnevskaya Elena,
Rizzuto Valeria,
PayánPernía Salvador,
Remacha Ángel,
Torrent Montserrat,
Ruiz Anna,
Badell Isabel,
Vives Corrons JoanLluis
Publication year - 2020
Publication title -
international journal of laboratory hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.705
H-Index - 55
eISSN - 1751-553X
pISSN - 1751-5521
DOI - 10.1111/ijlh.13110
Subject(s) - medicine , pyruvate kinase deficiency , library science , university hospital , hematologic neoplasms , family medicine , pyruvate kinase , cancer , computer science , glycolysis , metabolism
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