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Nature Cell Biology|June 5, 2012
Genome-wide RNAi screening identifies human proteins with a regulatory function in the early secretory pathwayJeremy C Simpson, Brigitte Joggerst, Vibor Laketa, et al.
Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.
Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.
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