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January 1, 1999Human Mutation

Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox

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PPPablo J. Pati�oJPJ. Eduardo PérezUniversity of PennsylvaniaJLJuan Álvaro López

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Cite This Study

Pati�o et al. (1999) studied this question.

synapsesocial.com/papers/6a6b7ca36f523709a024a756https://doi.org/10.1002/(sici)1098-1004(1999)13:1<29::aid-humu3>3.0.co;2-x
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.1994 · 70 citations
  2. 2Characterization of the p67phox gene: genomic organization and restriction fragment length polymorphism analysis for prenatal diagnosis in chronic granulomatous disease1993 · 37 citations