Point mutations in the beta-subunit of cytochrome b558 leading to X- linked chronic granulomatous disease

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease1989 · 172 citations
2. 2Nsi I RFLP at the X-linked chronic granulomatous disease locus (CYBB)1989 · 25 citations
3. 3Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus1988 · 53 citations
4. 4Two Forms of Autosomal Chronic Granulomatous Disease Lack Distinct Neutrophil Cytosol Factors1988 · 337 citations
5. 5Identification of the haem-binding subunit of cytochrome <i>b</i>−2451989 · 49 citations