A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred.
Calabresi L, Nilsson P, Pinotti E, Gomaraschi M, Favari E, Adorni MP, Bernini F, Sirtori CR, Calandra S, Franceschini G, Tarugi P.
Calabresi L, et al. Among authors: sirtori cr.
Atherosclerosis. 2009 Aug;205(2):506-11. doi: 10.1016/j.atherosclerosis.2009.01.006. Epub 2009 Jan 15.
Atherosclerosis. 2009.
PMID: 19200546