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Molecular analysis of chronic granulomatous disease and site-direted mutagenesis as models to solve the naden oxidase puzzle

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dc.contributor.authorCurnutte, John T.
dc.contributor.authorPérez, Juan E.
dc.contributor.authorLópez, Juan A.
dc.contributor.authorCondino Neto, Antonio
dc.contributor.authorGrumach, Anete S.
dc.contributor.authorBotero, Jorge H.
dc.contributor.authorCornejo de L., Mónica
dc.contributor.authorNavarro V., Sara
dc.contributor.authorDing, Jiabing
dc.contributor.authorGarcía Olarte, Diana
dc.contributor.authorRoesler, Joachim
dc.contributor.authorRae, Julie
dc.contributor.authorBarrett, David
dc.contributor.authorChanock, Stephen J.
dc.contributor.authorGoerlach, Agnes
dc.contributor.authorNoack, Deborah
dc.contributor.authorErickson, Rich
dc.contributor.corporationUniversidad de Antioquia.
dc.creator.authorPatiño Grajales, Pablo Javier
dc.date.accessioned2019-03-04T04:15:05Z
dc.date.available2019-03-04T04:15:05Z
dc.date.issued1993
dc.description.contentARTICULO(S) EN REVISTA: Recombination events between the p47 phox gene andits highly homologous pseudogenes;are the main cause of autosomal recessive chronic granulomatusdisease / Joachim Roesler ... [et al.]. -- En:;Blood. -- Vol.95, no. 6 (Mar. 2000); p. 2150-2156. -- Molecularcharacterization of autosomal recessive;chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate (reduced;form) oxidase component p67 phox / Pablo J. Patiño ... [etal.].'-- en: Blood. -- Vol. 94, no. 7 (1999); p.;2505-2514. -- Molecular analysis of chronic granulomatousdisease caused by defects in gp91 phox / Pablo J.;Patiño ... [et al.]. -- En: Human Mutation. -- no. 13 (1999);p.29-37. --Caracterizacion clinico molecular;de la enfermedad granulomatosa cronica autosomica recesivacausada por deficit de p47-phox / Monica Cornejo de;L. --- [et al.]. -- En: Revista Medica de Chile. -- Vol. 128 (2000); p.490-498.
dc.description.projectidIP 1115-04-476-96
dc.format.dimensions28 cm.
dc.format.extent19 h.
dc.identifier.urihttps://repositorio.minciencias.gov.co/handle/20.500.14143/33012
dc.publisher.nameUniversidad de Antioquia,
dc.publisher.placeMedellin :
dc.titleMolecular analysis of chronic granulomatous disease and site-direted mutagenesis as models to solve the naden oxidase puzzle
dspace.entity.typePublication

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