Titre:
  • Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
Auteur:Van Nieuwenhove, Erika; Barber, John J.S.; Neumann, Julika; Smeets, Elien; Willemsen, Mathijs; Pasciuto, Emanuela; Prezzemolo, Teresa; Lagou, Vasiliki; Seldeslachts, Laura; Malengier-Devlies, Bert; Metzemaekers, Mieke; Haßdenteufel, Sarah; Kerstens, Axelle; Van Der Kant, Rob; Rousseau, Frédéric; Schymkowitz, Joost J.; Di Marino, Daniele; Lang, Sven; Zimmermann, Richard; Schlenner, Susan; Munck, Sebastian; Proost, Paul; Matthys, Patrick; Devalck, Christine; Boeckx, Nancy; Claessens, Frank; Wouters, Carine; Humblet-Baron, Stéphanie; Meyts, Isabelle; Liston, Adrian
Informations sur la publication:Journal of allergy and clinical immunology
Statut de publication:Publié, 2020
Sujet CREF:Immunologie
Allergie et immunopathologie
Mots-clés:endoplasmic reticulum stress
SEC61A1
Severe congenital neutropenia
unfolded protein response
whole exome sequencing
Note générale:SCOPUS: ar.j
Langue:Anglais
Identificateurs:urn:issn:0091-6749
info:doi/10.1016/j.jaci.2020.03.034
info:pii/S0091674920304887
info:scp/85084657431
info:pmid/32325141