Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency. [electronic resource]
Producer: 20000808Description: 473-81 p. digitalISSN:- 0340-6717
- Base Sequence
- DNA -- genetics
- DNA Mutational Analysis
- DNA Primers -- genetics
- Female
- Granulomatous Disease, Chronic -- enzymology
- Humans
- Japan
- Male
- Membrane Glycoproteins -- deficiency
- Membrane Transport Proteins
- Mutation
- NADPH Dehydrogenase -- deficiency
- NADPH Oxidase 2
- NADPH Oxidases
- Phosphoproteins -- deficiency
- X Chromosome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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