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De novoCIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases
Author(s) -
Ivona Aksentijevich,
Miroslawa Nowak,
Mustapha Mallah,
Jae Jin Chae,
Wendy T. Watford,
Sigrun R. Hofmann,
Leonard I. Stein,
Ricardo Russo,
Donald Goldsmith,
Peter B. Dent,
Helene F. Rosenberg,
Frances Austin,
Elaine F. Remmers,
James E. Balow,
Sergio D. Rosenzweig,
Hirsh D. Komarow,
Nitza G. Shoham,
Geryl Wood,
J. B. Jones,
Nadira Mangra,
Hector Carrero,
Barbara S. Adams,
Terry L. Moore,
Kenneth N. Schikler,
Hal M. Hoffman,
Daniel J. Lovell,
Robert Lipnick,
Karyl S. Barron,
John J. O’Shea,
Daniel L. Kastner,
Raphaela GoldbachMansky
Publication year - 2002
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/qnf6-eb65
Subject(s) - pyrin domain , disease , immunology , genetic heterogeneity , medicine , genetics , inflammasome , inflammation , biology , gene , phenotype

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