Congenital Hemolytic Anemia Due to Hexokinase Deficiency
Author:
Publisher
American Medical Association (AMA)
Subject
Pediatrics, Perinatology, and Child Health
Cited by 7 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. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family;Journal of Clinical Pathology;2020-12-25
2. De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment;European Journal of Human Genetics;2019-02-18
3. Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1;Blood Cells, Molecules, and Diseases;2016-07
4. Gene Expression and Biological Significance of Hexokinase in Erythroid Cells;Acta Haematologica;2002
5. Hexokinase: gene structure and mutations;Best Practice & Research Clinical Haematology;2000-03
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