Zobrazeno 1 - 1
of 1
pro vyhledávání: '"SCN, Severe congenital neutropenia"'
Autor:
Mieke Metzemaekers, Susan M. Schlenner, Emanuela Pasciuto, Patrick Matthys, Stephanie Humblet-Baron, Elien Smeets, Adrian Liston, Axelle Kerstens, Joost Schymkowitz, Laura Seldeslachts, Paul Proost, Sarah Haßdenteufel, Carine Wouters, Frank Claessens, Julika Neumann, Teresa Prezzemolo, Nancy Boeckx, Vasiliki Lagou, John S. Barber, Frederic Rousseau, Bert Malengier-Devlies, Rob van der Kant, Erika Van Nieuwenhove, Christine Devalck, Isabelle Meyts, Sven Lang, Richard Zimmermann, Daniele Di Marino, Sebastian Munck, Mathijs Willemsen
Publikováno v:
Journal of allergy and clinical immunology
The Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology
The Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology
Background: The molecular cause of severe congenital neutropenia (SCN) is unknown in 30% to 50% of patients. SEC61A1 encodes the α-subunit of the Sec61 complex, which governs endoplasmic reticulum protein transport and passive calcium leakage. Recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4167ed5c5db874f50ba44ce06bf3f6
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307196
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307196
