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Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)

Dirk Roos, Karin van Leeuwen, Amy P. Hsu, Debra Long Priel, Amber Begtrup, Rhonda Brandon, Amit Rawat, Pandiarajan Vignesh, Manisha Madkaikar, Marie José Stasia, Faris G. Bakri, Martin de Boer, Joachim Roesler, Nezihe Köker, Mustafa Yavuz Köker, Marianne Antonius Jakobsen, Jacinta Bustamante, María Bravo García‐Morato, Juan Luis Valdivieso Shephard, Deniz Çağdaş, İlhan Tezcan, Roya Sherkat, Esmaeil Mortaz, Abbas Fayezi, Mohammad Shahrooei, Baruch Wolach, Lizbeth Blancas‐Galicia, Hirokazu Kanegane, Toshinao Kawai, Antônio Condino‐Neto, Mauno Vihinen, Christa S. Zerbe, Steven M. Holland, Harry L. Malech, John I. Gallin, Douglas B. Kuhns

2021Blood Cells Molecules and Diseases44 citationsDOI

Topics & Concepts

Chronic granulomatous diseaseNADPH oxidaseP22phoxGeneBiologyPrimary immunodeficiencySuperoxideGeneticsOxidase testCLPBReactive oxygen speciesMolecular biologyImmunologyEnzymeBiochemistryImmune systemMutantNeutrophil, Myeloperoxidase and Oxidative MechanismsS100 Proteins and AnnexinsInflammasome and immune disorders
Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update) | Litcius