Two new mutations of the glucose‐6‐phospate dehydrogenase (G6PD) gene associated with haemolytic anaemia: clinical, biochemical and molecular relationships
Author:
Affiliation:
1. Haematology Laboratory,
2. Department of Haematology and Haemotherapy, Hospital Universitario de Guadalajara, Madrid, Spain
3. General Internal Medicine Departments, Hospital Clinic i Provincial, Barcelona, Catalonia,
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2141.1997.2563071.x
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. An Overall View of the Functional and Structural Characterization of Glucose-6-Phosphate Dehydrogenase Variants in the Mexican Population;International Journal of Molecular Sciences;2023-08-11
2. Human G6PD variant structural studies: Elucidating the molecular basis of human G6PD deficiency;Gene Reports;2022-06
3. Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency;Anemia;2021-02-09
4. Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency;Annals of Laboratory Medicine;2017-03-01
5. The Stability of G6PD Is Affected by Mutations with Different Clinical Phenotypes;International Journal of Molecular Sciences;2014-11-17
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