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lüll Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease Roos D; de Boer M; Kuribayashi F; Meischl C; Weening RS; Segal AW; Ahlin A; Nemet K; Hossle JP; Bernatowska-Matuszkiewicz E; Middleton-Price HBlood 1996[Mar]; 87 (5): 1663-81ä|*Membrane Transport Proteins[MESH]|Base Sequence[MESH]|Cell Membrane/enzymology[MESH]|Chromosomes, Human, Pair 1/genetics[MESH]|Chromosomes, Human, Pair 16/genetics[MESH]|Chromosomes, Human, Pair 7/genetics[MESH]|Consensus Sequence[MESH]|Cytochrome b Group/chemistry/*deficiency/genetics[MESH]|Cytoplasmic Granules/enzymology[MESH]|Female[MESH]|Genes, Recessive[MESH]|Genetic Heterogeneity[MESH]|Genetic Therapy[MESH]|Granulomatous Disease, Chronic/classification/enzymology/*genetics/therapy[MESH]|Humans[MESH]|Interferon-gamma/therapeutic use[MESH]|Leukocytes/enzymology/ultrastructure[MESH]|Male[MESH]|Membrane Glycoproteins/*genetics[MESH]|Models, Molecular[MESH]|Molecular Sequence Data[MESH]|Mutation[MESH]|NADH, NADPH Oxidoreductases/chemistry/*deficiency/genetics[MESH]|NADPH Dehydrogenase/*genetics[MESH]|NADPH Oxidase 2[MESH]|NADPH Oxidases[MESH]|Phosphoproteins/*genetics[MESH]|Protein Conformation[MESH]|Recombinant Proteins[MESH]|Sequence Deletion[MESH]|X Chromosome/*genetics[MESH] |