Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
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Van Nieuwenhove E, et al. Among authors: van der kant r.
J Allergy Clin Immunol. 2020 Nov;146(5):1180-1193. doi: 10.1016/j.jaci.2020.03.034. Epub 2020 Apr 20.
J Allergy Clin Immunol. 2020.
PMID: 32325141
Free PMC article.