Defective SEC61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

scientific article published on 20 April 2020

Defective SEC61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.JACI.2020.03.034
P932PMC publication ID7649975
P698PubMed publication ID32325141

P50authorPaul ProostQ54449101
Carine WoutersQ77393750
Laura SeldeslachtsQ93181425
P2093author name stringRichard Zimmermann
Sven Lang
Teresa Prezzemolo
Patrick Matthys
Frederic Rousseau
Joost Schymkowitz
Frank Claessens
Vasiliki Lagou
Christine Devalck
Isabelle Meyts
Nancy Boeckx
Adrian Liston
Stephanie Humblet-Baron
Daniele Di Marino
Sebastian Munck
John S Barber
Emanuela Pasciuto
Bert Malengier-Devlies
Mieke Metzemaekers
Julika Neumann
Rob van der Kant
Sarah Haßdenteufel
Erika Van Nieuwenhove
Elien Smeets
Mathijs Willemsen
Axelle Kerstens
Susan Schlenner
P2860cites workSUMO modification regulates MafB-driven macrophage differentiation by enabling Myb-dependent transcriptional repressionQ35950115
P4510describes a project that usesImageJQ1659584
P921main subjectsevere congenital neutropeniaQ18553325
autosomal dominant severe congenital neutropeniaQ102293466
P577publication date2020-04-20
P1433published inThe Journal of Allergy and Clinical ImmunologyQ7743550
P1476titleDefective SEC61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

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