Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in neonates in Wuhan: Description of four novel variants

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common X-linked enzymopathies caused by G6PD gene variant. The aim of this study was to investigate the molecular epidemiological characteristic of the G6PD deficiency among newborn screening population in Wuhan region. A total o...

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Bibliografische gegevens

Hoofdauteurs:	Shanshan Shen, Qian Xiong, Wenqian Cai, Rui Hu, Bin Zhou, Xijiang Hu
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Frontiers Media S.A. 2022-09-01
Reeks:	Frontiers in Genetics
Onderwerpen:	G6PD variant G6PD genetic newborn screening novel variants Wuhan
Online toegang:	https://www.frontiersin.org/articles/10.3389/fgene.2022.994015/full
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