1. The ABCA subclass of mammalian transporters;Broccardo;Biochim. Biophys. Acta.,1999
2. Assman, G., von Eckardstein, A., Brewer, H. B., Jr, . 2001. Familial Analphalipoproteinemia: Tangier Disease. In, The Metabolic and Molecular Bases of Inherited Disease. Scriver, C. R., Beaudet, A. L., Sly, W. S., Valle, D., Childs, B., Kinzler, K. W., Volkman, B. F., editors. McGraw-Hill, New York. 2937–2960.
3. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency;Brooks-Wilson;Nat. Genet.,1999
4. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1;Rust;Nat. Genet.,1999
5. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease;Bodzioch;Nat. Genet.,1999