Coinheritance of a novel mutation on the HBA1 gene: c.187delG (p.W62fsX66) [codon 62 (-G) (α1)] with the α212 patchwork allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T].

Autor: Scheps KG; Cátedra de Genética y Biología Molecular, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina., De Paula SM, Bitsman AR, Freigeiro DH, Basack FN, Pennesi SP, Varela V

Publikováno v: Hemoglobin [Hemoglobin] 2013; Vol. 37 (5), pp. 492-500. Date of Electronic Publication: 2013 Jun 27.