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43. Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. Fasano T; Zanoni P; Rabacchi C; Pisciotta L; Favari E; Adorni MP; Deegan PB; Park A; Hlaing T; Feher MD; Jones B; Uzak AS; Kardas F; Dardis A; Sechi A; Bembi B; Minuz P; Bertolini S; Bernini F; Calandra S Mol Genet Metab; 2012 Nov; 107(3):534-41. PubMed ID: 22959828 [TBL] [Abstract][Full Text] [Related]
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57. An ABCA1 truncation shows no dominant negative effect in a familial hypoalphalipoproteinemia pedigree with three ABCA1 mutations. Sorrenson B; Suetani RJ; Bickley VM; George PM; Williams MJ; Scott RS; McCormick SP Biochem Biophys Res Commun; 2011 Jun; 409(3):400-5. PubMed ID: 21575609 [TBL] [Abstract][Full Text] [Related]
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