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Bibliografía
[1.]
D. Baldassarre, M. Amato, L. Pustina, E. Tremoli, C.R. Sirtori, L. Calabresi, et al.
Increased carotid artery intima-media thickness in subjects with hypoalphalipoproteinemia.
Arterioscler Thromb Vasc Biol, 22 (2002), pp. 317-322
[2.]
K. Yamakawa-Kobayashi, H. Yanagi, H. Fukayama, C. Hirano, Y. Shima, N. Yamamoto, et al.
Frequent ocurrence of hypoalphaliproteinemia due to mutant apolipoprotein A-I gene in the population: a population- base survey.
Human Mol Genet, 8 (1999), pp. 331-336
[3.]
D.C. McManus, B.R. Scott, V. Frankliln, D.L. Sparks, Y.L. Marcel.
Proteolytic degradation and impaired secretion of an apolipoprotein A-I mutant associated with dominantly inherited hypoalphalipoproteinemia.
J Biol Chem, 276 (2001), pp. 292-302
[4.]
J.M. Martín-Campos, J. Julve, J.C. Escola, J. Ordóñez-Llanos, J. Gómez, J. Binimelis, et al.
Apo A-I (MALLORCA) impairs LCAT activation and induces dominant familiar hypoalphalipoproteinemia.
J Lipi Res, 43 (2000), pp. 115-123
[5.]
H.E. Miettinen, H. Gylling, J. Tenhunen, J. Virtamo, M. Jauhianen, J.K. Huttunen, et al.
Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCATFin) of lecithin:cholesterol acytransferasa (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels.
Arterioscler Thromb Vasc Biol, 18 (1998), pp. 591-598
[6.]
M. Pocoví, A. Cenarro, F. Civeira, M.A. Torralba, J.I. Pérez-Calvo, P. Mozas, et al.
Beta-glucocerebrosidase gene locus as a link for Gaucher’s disease and familiar hypo-alpha-lipoproteinemia.
Lancet, 351 (1998), pp. 1919-1923
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