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Autor:
Harald Petry, Claus Sundgreen, Hans U. Klor, Erik S.G. Stroes, Karl Winkler, Anja Vogt, Pavlina Konstantinova, Deyanira Corzo, Rute Rodrigues, John D. Brunzell, Christian Meyer, Antonio Martínez, Sabine Westphal, Elisabeth Steinhagen-Thiessen, Ulrich Julius, Børge G. Nordestgaard, Diego Tejedor, Samir S. Deeb, Marta Artieda, Heinrich Prophet, Britta Otte, Phillip Hardt, Ioanna Gouni-Berthold
Publikováno v:
Journal of clinical lipidology, 10(2), 394-409. Elsevier BV
Background Lipoprotein lipase (LPL) deficiency is a serious lipid disorder of severe hypertriglyceridemia (SHTG) with chylomicronemia. A large number of variants in the LPL gene have been reported but their influence on LPL activity and SHTG has not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e60b0b5c5588710e8fd9144685866f64
https://doi.org/10.1016/j.jacl.2015.12.015
https://doi.org/10.1016/j.jacl.2015.12.015
