A combination of the -α3.7 and --MEDII alleles causing hemoglobin H disease in a Brazilian patient.

Autor: Dorta Ferreira, Roberta, de Oliveira Mota, Natália, Myiuki Kimura, Elza, Pedroso, Gisele Audrei, de Fatima Sonati, Maria
Předmět:
Zdroj: Brazilian Journal of Hematology & Hemotherapy / Revista Brasileira de Hematologia e Hemoterapia; Jan-Mar2017, Vol. 39 Issue 1, p80-83, 4p
Abstrakt: The article describes the case of a Brazilian patient with hemoglobin H disease caused by the combination of the -α3.7 deletion, the most common cause of alpha-thalassemia.
Databáze: Complementary Index