Glucosephosphate Isomerase (GPI) Deficiency Mutations Associated with Hereditary Nonspherocytic Hemolytic Anemia (HNSHA)
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
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4. Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia;Baronciani;Proc Natl Acad Sci USA,1993
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1. Genetic Analysis of Two Novel GPI Variants Disrupting H Bonds and Localization Characteristics of 55 Gene Variants Associated with Glucose-6-phosphate Isomerase Deficiency;Current Medical Science;2024-04
2. Glucose 6 Phosphate Isomerase Deficiency, a Rare Hemolytic Anemia Misdiagnosed as Hereditary Spherocytosis;Journal of Pediatric Hematology/Oncology;2022-09-12
3. Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report;BMC Pediatrics;2022-08-01
4. Hemolytic Anemia and Neurological Manifestations – An Uncommon Combination;The Indian Journal of Pediatrics;2019-06-10
5. Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases;Frontiers in Physiology;2019-05-07
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