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23. Tangier disease: epidemiology, pathophysiology, and management. Puntoni M; Sbrana F; Bigazzi F; Sampietro T Am J Cardiovasc Drugs; 2012 Oct; 12(5):303-11. PubMed ID: 22913675 [TBL] [Abstract][Full Text] [Related]
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26. ABC1: connecting yellow tonsils, neuropathy, and very low HDL. Hobbs HH; Rader DJ J Clin Invest; 1999 Oct; 104(8):1015-7. PubMed ID: 10525038 [No Abstract] [Full Text] [Related]
27. Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 ( ABCA1) gene in Japanese patients with Tangier disease. Guo Z; Inazu A; Yu W; Suzumura T; Okamoto M; Nohara A; Higashikata T; Sano R; Wakasugi K; Hayakawa T; Yoshida K; Suehiro T; Schmitz G; Mabuchi H J Hum Genet; 2002; 47(6):325-9. PubMed ID: 12111381 [TBL] [Abstract][Full Text] [Related]
28. A novel missense mutation of ABCA1 in transmembrane alpha-helix in a Japanese patient with Tangier disease. Maekawa M; Kikuchi J; Kotani K; Nagao K; Odgerel T; Ueda K; Kawano M; Furukawa Y; Sakurabayashi I Atherosclerosis; 2009 Sep; 206(1):216-22. PubMed ID: 19344898 [TBL] [Abstract][Full Text] [Related]
32. A novel homozygous ABCA1 variant in an asymptomatic man with profound hypoalphalipoproteinemia. Carcora Y; Brook RD; Farhat L; Willer CJ; Rubenfire M; Kim DS J Clin Lipidol; 2018; 12(4):878-882. PubMed ID: 29773422 [TBL] [Abstract][Full Text] [Related]
33. Promoter haplotype of a new ABCA1 mutant influences expression of familial hypoalphalipoproteinemia. Slatter TL; Williams MJ; Frikke-Schmidt R; Tybjaerg-Hansen A; Morison IM; McCormick SP Atherosclerosis; 2006 Aug; 187(2):393-400. PubMed ID: 16225879 [TBL] [Abstract][Full Text] [Related]
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35. Can Tangier disease cause male infertility? A case report and an overview on genetic causes of male infertility and hormonal axis involved. Stocchi L; Giardina E; Varriale L; Sechi A; Vagnini A; Parri G; Valentini M; Capalbo M Mol Genet Metab; 2018 Jan; 123(1):43-49. PubMed ID: 29198592 [TBL] [Abstract][Full Text] [Related]
36. Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis. Ishii J; Nagano M; Kujiraoka T; Ishihara M; Egashira T; Takada D; Tsuji M; Hattori H; Emi M J Hum Genet; 2002; 47(7):366-9. PubMed ID: 12111371 [TBL] [Abstract][Full Text] [Related]
37. Expression of the ATP-binding cassette transporter gene ABCG1 (ABC8) in Tangier disease. Lorkowski S; Kratz M; Wenner C; Schmidt R; Weitkamp B; Fobker M; Reinhardt J; Rauterberg J; Galinski EA; Cullen P Biochem Biophys Res Commun; 2001 May; 283(4):821-30. PubMed ID: 11350058 [TBL] [Abstract][Full Text] [Related]
38. Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. Bocchi L; Pisciotta L; Fasano T; Candini C; Puntoni MR; Sampietro T; Bertolini S; Calandra S Clin Chim Acta; 2010 Apr; 411(7-8):524-30. PubMed ID: 20093111 [TBL] [Abstract][Full Text] [Related]
39. Peripheral neuropathy in Tangier disease. Pollock M; Nukada H; Frith RW; Simcock JP; Allpress S Brain; 1983 Dec; 106 ( Pt 4)():911-28. PubMed ID: 6317140 [TBL] [Abstract][Full Text] [Related]
40. Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population? Pajukanta P J Clin Invest; 2004 Nov; 114(9):1244-7. PubMed ID: 15520856 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]