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Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease – Identification of Eight Novel Mutations in CYBB and NCF2 Genes

Genetic AnalysisAutoimmune DiseaseConnective Tissue DiseaseGranulocyteGenetic DisorderImmunodeficienciesEight Novel MutationsPathologyDisease Gene IdentificationDermatologyMedicineClinical GeneticsNcf2 Genes