Sec61a1-flox 基因敲除小鼠

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4. Van Nieuwenhove, Erika, Barber, John S, Neumann, Julika, Meyts, Isabelle, Liston, Adrian. 2020. Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia. In The Journal of allergy and clinical immunology, 146, 1180-1193. doi:10.1016/j.jaci.2020.03.034. https://pubmed.ncbi.nlm.nih.gov/32325141/