Prevalência da deficiência de G6PD e caracterização molecular dos polimorfismos G202A, A376G e C563T em neonatos no Sudeste do Brasil.

Autor: Dias Pereira, Lucas Luís Meigre¹, Augusta Bravin, Cristina², Sarquis Cintra, Terezinha³, Portela Cassa, Wélida Santos², Altoé Santos, Thainá², Fonseca, Armando⁴, Pratte-Santos, Rodrigo^1,5 rodrigopratte@hotmail.com

Publikováno v: Einstein (16794508). 2019, Vol. 17 Issue 1, p1-7. 7p.

Prevalence of G6PD deficiency and molecular characterization of G202A, A376G and C563T polymorphisms in newborns in Southeastern Brazil

Autor: Pereira, Lucas Luís Meigre Dias, Bravin, Cristina Augusta, Cintra, Terezinha Sarquis, Cassa, Wélida Santos Portela, Santos, Thainá Altoé, Fonseca, Armando, Pratte-Santos, Rodrigo

Publikováno v: Einstein
einstein (São Paulo) v.17 n.1 2019
Einstein (São Paulo)
Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron:IIEPAE
Einstein (São Paulo), Vol 17, Iss 1

Objective To evaluate the prevalence of G6PD deficiency and characterize G202A, A376G and C563T polymorphisms in neonates using molecular assays. Methods A total of one thousand samples were tested through quantitative analysis of enzyme activity, de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83ffd76a4983628e736fc42da741a4d3
https://doi.org/10.31744/einstein_journal/2019ao4436