ϵγ-Thalassemia, a New Hemoglobinopathy Category.

BACKGROUND: Large β-globin gene cluster deletions (hereditary persistence of fetal hemoglobin [Hb] or β-, δβ-, γδβ-, and ϵγδβ-thalassemia), are associated with widely disparate phenotypes, including variable degrees of microcytic anemia and Hb F levels. When present, increased Hb A2 is used as a sur...

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Publicado en:	Clinical Chemistry Vol. 69; no. 7; pp. 711 - 718
Autores principales:	Oliveira, Jennifer L., Thompson, Christineil H., Saravanaperumal, Siva Arumugam, Koganti, Tejaswi, Jenkinson, Garrett, Hein, Molly S., Kohorst, Mira A., Hasadsri, Linda, Nguyen, Phuong L., Matern, Dietrich, Kipp, Benjamin R., Klee, Eric W., Wieben, Eric D., Hoyer, James D., Rangan, Aruna
Formato:	Journal Article
Publicado:	Oxford University Press / USA Jul2023
Acceso en línea:	Ver este registro en EBSCOhost