Corrigendum: Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization

[...] an earlier study (ref. 20 in the original manuscript) reported functional analyses of the C14ORF133 gene product (also called SPE-39), described the generation of a polyclonal antibody against human SPE-39 and reported an interaction between SPE-39 and VPS33B, similar to the interaction shown in Figure 1b.