Title : Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project - Kim_2014_J.Lipid.Res_55_1173 |
Author(s) : Kim DS , Crosslin DR , Auer PL , Suzuki SM , Marsillach J , Burt AA , Gordon AS , Meschia JF , Nalls MA , Worrall BB , Longstreth WT, Jr. , Gottesman RF , Furlong CE , Peters U , Rich SS , Nickerson DA , Jarvik GP |
Ref : J Lipid Res , 55 :1173 , 2014 |
Abstract : |
PubMedSearch : Kim_2014_J.Lipid.Res_55_1173 |
PubMedID: 24711634 |
Title : Genetic polymorphisms of microsomal and soluble epoxide hydrolase and the risk of Parkinson's disease - Farin_2001_Pharmacogenet_11_703 |
Author(s) : Farin FM , Janssen P , Quigley S , Abbott D , Hassett C , Smith-Weller T , Franklin GM , Swanson PD , Longstreth WT, Jr. , Omiecinski CJ , Checkoway H |
Ref : Pharmacogenetics , 11 :703 , 2001 |
Abstract : |
PubMedSearch : Farin_2001_Pharmacogenet_11_703 |
PubMedID: 11692079 |