Publication: Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus
Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus
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Frey, D., Mächler, M., Seger, R., Schmid, W., & Orkin, S. H. (1988). Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus. Blood, 71, 252–255. https://doi.org/10.1182/blood.V71.1.252.252
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In a patient suffering from X-linked chronic granulomatous disease (X- CGD)--a disorder of phagocytesuperoxide generation--and McLeod syndrome, characterized by the absence of the red cell Kell antigen, we identified a deletion of the entire X-CGD gene by means of DNA hybridization with a cDNA probe. Our findings suggest that the X-CGD and McLeod loci are physically close in the p21 region of the X chromosome proximal to the Duchenne muscular dystrophy locus.
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- Frey, Daniel
- Mächler, Marco
- Seger, Reinhard
- Schmid, Werner
- Orkin, Stuart H.
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Frey, D., Mächler, M., Seger, R., Schmid, W., & Orkin, S. H. (1988). Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus. Blood, 71, 252–255. https://doi.org/10.1182/blood.V71.1.252.252
