[1] SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects.Nat Commun. 2018 Aug 6;9(1):3087.

[2] Molecular and phylogenetic characterization of a novel putative membrane transporter (SLC10A7), conserved in vertebrates and bacteria.Eur J Cell Biol. 2007 Aug;86(8):445-60.

[3] Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation.Hum Mol Genet. 2018 Sep 1;27(17):3029-3045.