| 1 | LPA, LPAL2, SLC22A3 |
| Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. | |
| Trégouët DA, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Grosshennig A, Linsel-Nitschke P, Perret C, DeSuremain M, Meitinger T, Wright BJ, Preuss M, Balmforth AJ, Ball SG, Meisinger C, Germain C, Evans A, Arveiler D, Luc G, Ruidavets JB, Morrison C, van der Harst P, Schreiber S, Neureuther K, Schäfer A, Bugert P, El Mokhtari NE, Schrezenmeir J, Stark K, Rubin D, Wichmann HE, Hengstenberg C, Ouwehand W; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Ziegler A, Tiret L, Thompson JR, Cambien F, Schunkert H, Samani NJ. | |
| Nat Genet 41(3):283-5. Epub 2009 Feb 8. 2009 | |
| 2 | LPAL2 |
| Loss of a splice donor site at a 'skipped exon' in a gene homologous to apolipoprotein(a) leads to an mRNA encoding a protein consisting of a single kringle domain. | |
| Byrne CD, Schwartz K, Lawn RM. | |
| Arterioscler Thromb Vasc Biol 15(1):65-70. 1995 | |
| 3 | LPA, LPAL1, LPAL2, TRDP |
| Molecular characterisation of the human apo(a)-plasminogen gene family clustered on the telomeric region of chromosome 6 (6q26-27). | |
| Magnaghi P, et al. | |
| Hum Mol Genet 3 : 437-442. 1994 | |