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Familial analphalipoproteinemia: Tangier disease. The Metabolic and Molecular Bases of Inherited Diseases (McGraw Hill),           2001; 8th ed. vol           2: 2937-2960"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2) Fredrickson DS, Altrocchi PH, Avioli LV, Goodman DS, Goodman HC. Tangier disease\u2014Combined clinical staff conference at the National Institutes of Health.           Ann Intern Med,           1961;           55: 1016-1031","DOI":"10.7326\/0003-4819-55-6-1016"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3) Hara H, Yokoyama S.          Interaction of free apolipoproteins with macrophages. Formation of high-density lipoprotein-like lipoproteins and reduction of cellular cholesterol.           J Biol Chem,           1991;           266: 3080-3086","DOI":"10.1016\/S0021-9258(18)49957-7"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4) Francis GA, Knopp RH, Oram JF.           Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier disease.           J Clin Invest,           1995;           96: 78-87","DOI":"10.1172\/JCI118082"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5) Brooks-Wilson A, Marcil M, Clee SM, Zhang LH, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HO, Loubser O, Ouelette BF, Fichter K, Ashbourne-Excoffon KJ, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone S, Kastelein JJ, Genest J Jr, Hayden MR .           Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.           Nat Genet,           1999;           22: 336-345","DOI":"10.1038\/11905"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6) Bodzioch M, Ors\u00f3 E, Klucken J, Langmann T, B\u00f6ttcher A, Diederich W, Drobnik W, Barlage S, B\u00fcchler C, Porsch-Ozc\u00fcr\u00fcmez M, Kaminski WE, Hahmann HW, Oette K, Rothe G, Aslanidis C, Lackner KJ, Schmitz G.          The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.           Nat Genet,           1999;           22: 347-351","DOI":"10.1038\/11914"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7) Rust S, Rosier M, Funke H, Real J, Amoura Z, Piette JC, Deleuze JF, Brewer HB, Duverger N, Den\u00e8fle P, Assmann G.          Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1.           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J Atheroscler Thromb,           2004;           11: 131-145","DOI":"10.5551\/jat.11.131"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10) Hooper AJ, McCormick S, Hegele RA, Burnett JR.          Clinical utility gene card for: Tangier disease.           Eur J Hum Genet,           2017;           25: e1-e3","DOI":"10.1038\/ejhg.2017.72"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11) Costet P, Luo Y, Wang N, Tall AR.           Sterol-dependent transactivation of the ABC1 promoter by the liver X receptor\/retinoid X receptor.           J Biol Chem,           2000;           275: 28240-28245","DOI":"10.1074\/jbc.M003337200"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12) Tamehiro N, Shigemoto-Mogami Y, Kakeya T, Okuhira K, Suzuki K, Sato R, Nagao T, Nishimaki-Mogami T.           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J Lipid Res,           2007;           48: 299-306","DOI":"10.1194\/jlr.M600428-JLR200"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17) Koseki M, Matsuyama A, Nakatani K, Inagaki M, Nakaoka H, Kawase R, Yuasa-Kawase M, Tsubakio-Yamamoto K, Masuda D, Sandoval JC, Ohama T, Nakagawa-Toyama Y, Matsuura F, Nishida M, Ishigami M, Hirano K, Sakane N, Kumon Y, Suehiro T, Nakamura T, Shimomura I, Yamashita S.          Impaired insulin secretion in four Tangier disease patients with ABCA1 mutations.           J Atheroscler Thromb,           2009;           16: 292-296","DOI":"10.5551\/jat.E599"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18) Brunham LR, Kruit JK, Pape TD, Timmins JM, Reuwer AQ, Vasanji Z, Marsh BJ, Rodrigues B, Johnson JD, Parks JS, Verchere CB, Hayden MR.          Beta-cell ABCA1 influences insulin secretion, glucose homeostasis and response to thiazolidinedione treatment.           Nat Med,           2007;           13: 340-347","DOI":"10.1038\/nm1546"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19) Schaefer EJ, Blum CB, Levy RI, Jenkins LL, Alaupovic P, Foster DM, Brewer HB Jr.           Metabolism of high-density lipoprotein apolipoproteins in Tangier disease.           N Engl J Med,           1978;           299: 905-910","DOI":"10.1056\/NEJM197810262991701"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20) Bi X, Pashos EE, Cuchel M, Lyssenko NN, Hernandez M, Picataggi A, McParland J, Yang W, Liu Y, Yan R, Yu C, DerOhannessian SL, Phillips MC, Morrisey EE, Duncan SA, Rader DJ.           ATP-binding cassette transporter A1 deficiency in human induced pluripotent stem cell-derived hepatocytes abrogates HDL biogenesis and enhances triglyceride secretion. 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