Neonatal Screening for Sickle Cell Disease in Congo

Neonatal Screening for Sickle Cell Disease in Congo

Introduction. Sickle cell disease is an autosomal recessive inherited disorder due to the mutation of a gene coding for the globin beta chain. The aim of this study is to update the epidemiological data on hemoglobinoses, in particular sickle cell disease in newborns in Congo. Materials and Methods....

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Main Authors: Alexis Elira Dokekias, Lethso Thibaut Ocko Gokaba, Josué Simo Louokdom, Lydie Ngolet Ocini, Firmine Olivia Galiba Atipo Tsiba, Coreillia Irène Ondzotto Ibatta, Quentin Ngoma Kouandzi, Serge Talomg Tamekue, Jayne Chelsea Bango, Jade Vanessa Nziengui Mboumba, Simon Charles Kobawila
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Anemia
Online Access:http://dx.doi.org/10.1155/2022/9970315
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http://dx.doi.org/10.1155/2022/9970315

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