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Novel mechanism of hereditary pyropoikilocytosis phenotype due to co-inheritance of β globin and α spectrin mutations.
Novel mechanism of hereditary pyropoikilocytosis phenotype due to co-inheritance of β globin and α spectrin mutations.
2021
Soo Jin Kim
Jihyun Song
N. Scott Reading
Julio Lautersztain
Abdullah Kutlar
Archana M. Agarwal
Theresa L. Coetzer
Josef T. Prchal
Keywords:
α spectrin
Genetics
Phenotype
Hereditary pyropoikilocytosis
Biology
Globin
Correction
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