Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose‐6‐phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm. (20th September 2019) - Krishnevskaya, Elena; Rizzuto, Valeria; Payán‐Pernía, Salvador; Remacha, Ángel; Torrent, Montserrat; Ruiz, Anna; Badell, Isabel; Vives Corrons, Joan‐Lluis