Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome

Autor: Felipe Suarez, Fran cois Tron, Nathalie Lambert, Vincent Barlogis, David Boutboul, Yvon Lebranchu, Celine Cazorla, Marie-Olivia Chandesris, Nizar Mahlaoui, Virginie Grandin, Isabelle Melki, Marianne Debré, Stephanie Ndaga, Olivier Hermine, Marguerite Micheau, Corinne Jacques, Gerard Body, Gilles Palenzuela, Christine Bodemer, Virginie Gandemer, Jean-Louis Stephan, Chantal Harre, Rolland Jaussaud, Anne Durandy, Stephane Dominique, Nathalie Aladjidi, Monique Forveille, Catherine Mathey, Martine Munzer, Capucine Picard, Brigitte Bader-Meunier, André Baruchel, Jean-Laurent Casanova, Muriel Le Bourgeois, Eric Oksenhendler, Ling Yun, Angels Natividad, Fanny Fouyssac, Cyrille Hoarau, Stéphane Blanche, Anne Puel, Caroline Thumerelle, Marie-Alexandra Alyanakian, Caroline Thomas, Alain Fischer, Claire Fieschi, Olivier Lortholary

Publikováno v: Medicine
Medicine, 2012, 91 (4), pp.e1-e19. ⟨10.1097/MD.0b013e31825f95b9⟩
Medicine, Lippincott, Williams & Wilkins, 2012, 91 (4), pp.e1-e19. 〈10.1097/MD.0b013e31825f95b9〉
Medicine, Lippincott, Williams & Wilkins, 2012, 91 (4), pp.e1-e19. ⟨10.1097/MD.0b013e31825f95b9⟩

International audience; ABSTRACT: Autosomal dominant deficiency of signal transducer and activator of transcription 3 (STAT3) is the main genetic etiology of hyper-immunoglobulin (Ig) E syndrome. We documented the molecular, cellular, and clinical fe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374240933d9fee7bdb71b68525757f49
https://doi.org/10.1097/md.0b013e31825f95b9