Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations. | EBSCOhost

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Title: Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations.
Authors: Kim, Soo Jin; Song, Jihyun; Reading, N. Scott; Lautersztain, Julio; Kutlar, Abdullah; Agarwal, Archana M.; Coetzer, Theresa L.; Prchal, Josef T.
Publication: American Journal of Hematology, 2021, Vol 96, Issue 5, pE150
ISSN: 0361-8609
Publication type: Academic Journal
DOI: 10.1002/ajh.26121