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Autor:
Paula Rq Estrada, Alex Mm Dias, Augusto M Azzolini, Gislaine S Pereira, Caio Graco Bruzaca, Kalina Rn Endo, Mariana Angelozzi de Oliveira, Ciro Dresch Martinhago, Ana Carolina Nogueira Martinhago
Publikováno v:
JBRA Assisted Reproduction
Sickle cell anemia is an inherited systemic hemoglobinopathy that affects hemoglobin production in red blood cells, leading to early morbidity and mortality. It is caused by a homozygous nucleotide substitution (c.20A>T) in the β-globin gene (HBB) t