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An unusual hemoglobinopathy: compound heterozygosity for hemoglobins C and E
Author(s) -
Chapman Michael Spencer,
Kiritkumar Kripesh,
Lund Kirstin,
Bain Barbara J.
Publication year - 2019
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.25309
Subject(s) - hemoglobin , hemoglobinopathy , compound heterozygosity , hemoglobin f , hemoglobin a2 , hemoglobin variants , asymptomatic , hemoglobin electrophoresis , hemoglobin e , soluble transferrin receptor , iron deficiency , medicine , chemistry , biochemistry , biology , anemia , genetics , hemolytic anemia , fetal hemoglobin , mutation , gene , pregnancy , fetus , iron status
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