Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency-Reference-Cited by-同舟云学术

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency

Published:2003-04 Issue:2 Volume:167 Page:335-345
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Pisciotta Livia,Miccoli Roberto,Cantafora Alfredo,Calabresi Laura,Tarugi Patrizia,Alessandrini Paola,Bittolo Bon Gabriele,Franceschini Guido,Cortese Claudio,Calandra Sebastiano,Bertolini Stefano

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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3. Apolipoprotein A-I: structure–function relationships;Frank;J. Lipid. Res.,2000

4. The apoAI-CIII-AIV gene cluster;Groenendijk;Atherosclerosis,2001

5. Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene;Matsunaga;Proc. Natl. Acad. Sci. USA,1991

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