Strom TB, Tveita AA, Bogsrud MP, Leren TP (2023) <br />Molecular genetic testing and measurement of levels of GPIHBP1 autoantibodies in patients with severe hypertriglyceridemia: The importance of identifying the underlying cause of hypertriglyceridemia<br /><i>J Clin Lipidol</i> <br /><br />Strom TB, Vinje T, Bjune K, da Costa LT, Laerdahl JK, Leren TP (2020) <br />Lysosomal acid lipase does not have a propeptide and should not be considered being a proprotein<br /><i>Proteins</i> <b>88</b>: 440<br /><br />Vinje T, Laerdahl JK, Bjune K, Leren TP, Strom TB (2019) <br />Characterization of the mechanisms by which missense mutations in the lysosomal acid lipase gene disrupt enzymatic activity<br /><i>Hum Mol Genet</i> <b>28</b>: 3043<br /><br />Vinje T, Wierod L, Leren TP, Strom TB (2018) <br />Prevalence of cholesteryl ester storage disease among hypercholesterolemic subjects and functional characterization of mutations in the lysosomal acid lipase gene<br /><i>Mol Genet Metab</i> <b>123</b>: 169<br /><br />Pingitore P, Lepore SM, Pirazzi C, Mancina RM, Motta BM, Valenti L, Berge KE, Retterstol K, Leren TP, Wiklund O, Romeo S (2016) <br />Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia<br /><i>J Clin Lipidol</i> <b>10</b>: 816<br /><br />Strom EH, Sund S, Reier-Nilsen M, Dorje C, Leren TP (2011) <br />Lecithin: Cholesterol Acyltransferase (LCAT) Deficiency: renal lesions with early graft recurrence<br /><i>Ultrastruct Pathol</i> <b>35</b>: 139<br /><br />Pasalic D, Jurcic Z, Stipancic G, Ferencak G, Leren TP, Djurovic S, Stavljenic-Rukavina A (2004) <br />Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia<br /><i>Clinica Chimica Acta</i> <b>343</b>: 179<br /><br />