Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification
Published 2023 View Full Article
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Title
Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification
Authors
Keywords
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Journal
BRITISH JOURNAL OF HAEMATOLOGY
Volume 202, Issue 5, Pages 1024-1032
Publisher
Wiley
Online
2023-07-07
DOI
10.1111/bjh.18943
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Related references
Note: Only part of the references are listed.- Functional interpretation, cataloging, and analysis of 1,341 glucose-6-phosphate dehydrogenase variants
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- Technical evaluation and usability of a quantitative G6PD POC test in cord blood: a mixed-methods study in a low-resource setting
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- Glucose-6-phosphate dehydrogenase activity in individuals with and without malaria: Analysis of clinical trial, cross-sectional and case–control data from Bangladesh
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- (2018) Lucio Luzzatto et al. NEW ENGLAND JOURNAL OF MEDICINE
- Pegloticase-Associated Hemolysis
- (2018) Marwan Abu Minshar et al. AMERICAN JOURNAL OF THERAPEUTICS
- Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community
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- Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range
- (2015) Xiang Wan et al. BMC Medical Research Methodology
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- (2012) Angelo Minucci et al. BLOOD CELLS MOLECULES AND DISEASES
- Quantitative Neonatal Glucose-6-Phosphate Dehydrogenase Screening: Distribution, Reference Values, and Classification by Phenotype
- (2012) Nurit Algur et al. JOURNAL OF PEDIATRICS
- Five novel glucose-6-phosphate dehydrogenase deficiency haplotypes correlating with disease severity
- (2012) Ashraf Dallol et al. Journal of Translational Medicine
- Lethal Effect of a Single Dose of Rasburicase in a Preterm Newborn Infant
- (2012) P. Zaramella et al. PEDIATRICS
- G6PD Deficiency Prevalence and Estimates of Affected Populations in Malaria Endemic Countries: A Geostatistical Model-Based Map
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