Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico

Hemoglobin S is caused by a nucleotide change in HBB gene (HBB:c.20A>T, p.Glu6Val), is presented in diverse forms: simple carriers (HbSA), homozygotes (HbSS) also known as sickle cell anemia, and compound heterozygotes with other β-hemoglobinopathies. It is worldwide distributed, in Mexico, is fr...

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Veröffentlicht in:	Journal of tropical pediatrics (1980) 2022-08, Vol.68 (5)
Hauptverfasser:	Rizo-de la Torre, L C, Borrayo-López, F J, Perea-Díaz, F J, Aquino, E, Venegas, M, Hernández-Carbajal, C, Espinoza-Mata, L L, Ibarra-Cortés, B
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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