LRP8
MIM.602600 1p34
apolipoprotein E receptor 2 APOER2
Pathology
Polymorphisms (gene variants) in
- maternal LRP8 gene associated with fetal growth restriction (FGR) (16642433)
- LRP8 variant associated with familial and premature coronary artery disease and myocardial infarction (17847002)
References
Shen GQ, Li L, Girelli D, Seidelmann SB, Rao S, Fan C, Park JE, Xi Q, Li J, Hu Y, Olivieri O, Marchant K, Barnard J, Corrocher R, Elston R, Cassano J, Henderson S, Hazen SL, Plow EF, Topol EJ, Wang QK. An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction. Am J Hum Genet. 2007 Oct;81(4):780-91. PMID: 17847002