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Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
Julie Toubiana, Satoshi Okada, Julia Hiller, Matias Oleastro, Macarena Lagos Gomez, Juan Carlos Aldave Becerra, Marie Ouachée-Chardin, Fanny Fouyssac, Katta Mohan Girisha, Amos Etzioni, Joris Van Montfrans, Yildiz Camcioglu, Leigh Ann Kerns, Bernd Belohradsky, Stéphane Blanche, Aziz Bousfiha, Carlos Rodriguez-Gallego, Isabelle Meyts, Kai Kisand, Janine Reichenbach
- Hôpital Necker Enfants Malades
- Univ-Paris Diderot Sorbonne Paris-Cité
- Université Paris Descartes
- Rockefeller University
- Hiroshima University Graduate School of Biomedical and Health Sciences
- Technical University of Munich
- Christine Kühne Center for Allergy Research and Education (CK-Care)
- Juan Pedro Garrahan National Hospital of Pediatrics
- Universidad de Valparaíso
- Edgardo Rebagliati Martins National Hospital
- Hôpital Robert Debré
- Hopital d'Enfants CHU Nancy
- Kasturba Medical College, Manipal
- Meyer Children's Hospital
- University Medical Center Utrecht
- Cerrahpasa Medical School
- Rainbow Babies and Children's Hospital
- Ludwig-Maximilians-Universität München
- King Hassan II University
- Hospital Universitario Son Espases
- Leuven University Center for Metabolic Bone Diseases
- University of Tartu
- University Children's Hospital Zurich
- National Institute of Allergy and Infectious Diseases (NIAID)
- University of Freiburg
- Amalia Children's Hospital
- University of Debrecen
- Tokyo Medical and Dental University
- Royal Victoria Infirmary
- Howard Hughes Medical Institute
Research output: Contribution to journal › Article › peer-review
421
Scopus
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