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Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations
Author(s) -
Kim Soo Jin,
Song Jihyun,
Reading N. Scott,
Lautersztain Julio,
Kutlar Abdullah,
Agarwal Archana M.,
Coetzer Theresa L.,
Prchal Josef T.
Publication year - 2021
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.26121
Subject(s) - frameshift mutation , genetics , nonsense mutation , biology , missense mutation , mutation , microcytosis , exon , nonsense mediated decay , phenotype , compound heterozygosity , thalassemia , gene , microbiology and biotechnology , anemia , medicine , iron deficiency , rna splicing , rna
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