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Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

Erika Van Nieuwenhove, John S. Barber, Julika Neumann, Elien Smeets, Mathijs Willemsen, Emanuela Pasciuto, Teresa Prezzemolo, Vasiliki Lagou, Laura Seldeslachts, Bert Malengier‐Devlies, Mieke Metzemaekers, Sarah Haßdenteufel, Axelle Kerstens, Rob van der Kant, Frédéric Rousseau, Joost Schymkowitz, Daniele Di Marino, Sven Lang, Richard Zimmermann, Susan Schlenner, Sebastian Munck, Paul Proost, Patrick Matthys, Christine Devalck, Nancy Boeckx, Frank Claessens, Carine Wouters, Stéphanie Humblet‐Baron, Isabelle Meyts, Adrian Liston

2020Journal of Allergy and Clinical Immunology46 citationsDOIOpen Access PDF

Topics & Concepts

NeutropeniaMedicineCongenital NeutropeniaIntensive care medicineInternal medicineChemotherapyBlood disorders and treatmentsErythrocyte Function and PathophysiologyGlycogen Storage Diseases and Myoclonus
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia | Litcius