Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose-6-phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm.
Elena KrishnevskayaValeria RizzutoSalvador Payán-PerníaÁngel RemachaMontserrat TorrentAnna RuizIsabel BadellJoan-Lluis Vives CorronsPublished in: International journal of laboratory hematology (2019)