A case of G6PD Utrecht associated with β‐thalassemia responding to splenectomy
Author:
Affiliation:
1. Department of Hematology Zigong First People's Hospital Zigong China
2. Department of Critical Medicine Zigong First People's Hospital Zigong China
3. Department of Pharmacy Zigong First People's Hospital Zigong China
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29837
Reference16 articles.
1. Glucose-6-phosphate dehydrogenase deficiency
2. Laboratory diagnosis of G6PD deficiency. A British Society for Haematology Guideline
3. Glucose-6-Phosphate Dehydrogenase Deficiency
4. Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase
5. Somatic‐cell selection is a major determinant of the blood‐cell phenotype in heterozygotes for glucose‐6‐phosphate dehydrogenase mutations causing severe enzyme deficiency;Filosa S;Am J Hum Genet,1996
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