Rapid detection of twenty-nine common Chinese glucose-6-phosphate dehydrogenase variants using a matrix-assisted laser desorption/ionization-time of flight mass spectrometry assay on dried blood spots-Reference-Cited by-同舟云学术

Rapid detection of twenty-nine common Chinese glucose-6-phosphate dehydrogenase variants using a matrix-assisted laser desorption/ionization-time of flight mass spectrometry assay on dried blood spots

Published:2021-08 Issue: Volume:94 Page:27-34
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Dai Weiqian^ORCID,Yang Tingting,Wang Yu,Zhao Qianfeng,Zhan Yongkun,Ye Jun,Han Lianshu,Qiu Wenjuan,Zhang Huiwen,Liang Lili,Gu Xuefan,Yu Yongguo

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference25 articles.

1. Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull. World Health Organiz.. 1989;67(6):601–611.

2. Glucose-6-phosphate dehydrogenase laboratory assay: how, when, and why?;Minucci;IUBMB Life,2009

3. Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates;Fu;Sci. Rep.,2018

4. Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China;Peng;PLoS ONE,2015

5. Neonatal screening for glucose-6-phosphate dehydrogenase deficiency: biochemical versus genetic technologies;Kaplan;Semin. Perinatol.,2011

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