[1] The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6.Nat Commun. 2016 Aug 10;7:12353.

[2] ABCB6 mutations cause ocular coloboma.Am J Hum Genet. 2012 Jan 13;90(1):40-8.

[3] Role of the N-terminal transmembrane domain in the endo-lysosomal targeting and function of the human ABCB6 protein.Biochem J. 2015 Apr 1;467(1):127-39.

[4] Shifting the paradigm: the putative mitochondrial protein ABCB6 resides in the lysosomes of cells and in the plasma membrane of erythrocytes.PLoS One. 2012;7(5):e37378.

[5] The human ABCB6 protein is the functional homologue of HMT-1 proteins mediating cadmium detoxification.Cell Mol Life Sci. 2019 Oct;76(20):4131-4144.

[6] ABCB6 Resides in Melanosomes and Regulates Early Steps of Melanogenesis Required for PMEL Amyloid Matrix Formation.J Mol Biol. 2018 Oct 12;430(20):3802-3818.

[7] Efficient purification and reconstitution of ATP binding cassette transporter B6 (ABCB6) for functional and structural studies.J Biol Chem. 2013 Aug 2;288(31):22658-69.

[8] Human ABCB6 localizes to both the outer mitochondrial membrane and the plasma membrane.Biochemistry. 2007 Aug 21;46(33):9443-52.