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A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease

Autoimmune DiseaseGranulocyteMedicineGeneticsInherited Metabolic DiseaseHematologyPathogenesisPathologyPoint MutationGenetic DisorderDisease Gene IdentificationGlutamic Acid