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Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1

Molecular CharacterizationGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseHematologyPathogenesisPathologyNovel MutationsNew CasesBlood CellMolecular GeneticsDisease Gene IdentificationHeme HomeostasisMolecular DiagnosticsCell Biology