المؤلفون: Lim, Et, Würtz, P, Havulinna, As, Palta, P, Tukiainen, T, Rehnström, K, Esko, T, Mägi, R, Inouye, M, Lappalainen, T, Chan, Y, Salem RM, Lek M, Flannick, J, Sim, X, Manning, A, Ladenvall, C, Bumpstead, S, Hämäläinen, E, Aalto, K, Maksimow, M, Salmi, M, Blankenberg, S, Ardissino, D, Shah, S, Horne, B, Mcpherson, R, Hovingh, Gk, Reilly, Mp, Watkins, H, Goel, A, Farrall, M, Reiner, Ap, Stitziel, No, Kathiresan, S, Gabriel, S, Barrett, Jc, Lehtimäki, T, Laakso, M, Groop, L, Kaprio, J, Perola, M, Mccarthy, Mi, Boehnke, M, Altshuler DM, Lindgren CM, Hirschhorn, Jn, Metspalu, A, Freimer, Nb, Zeller, T, Jalkanen, S, Koskinen, S, Raitakari, O, Durbin, R, Macarthur, Dg, Salomaa, V, Ripatti, S, Daly, Mj, Palotie, A, Sequencing, Initiative Suomi Project, GIRELLI, Domenico

المساهمون: Lim, Et, Würtz, P, Havulinna, A, Palta, P, Tukiainen, T, Rehnström, K, Esko, T, Mägi, R, Inouye, M, Lappalainen, T, Chan, Y, Salem RM, Lek M, Flannick, J, Sim, X, Manning, A, Ladenvall, C, Bumpstead, S, Hämäläinen, E, Aalto, K, Maksimow, M, Salmi, M, Blankenberg, S, Ardissino, D, Shah, S, Horne, B, Mcpherson, R, Hovingh, Gk, Reilly, Mp, Watkins, H, Goel, A, Farrall, M, Girelli, Domenico, Reiner, Ap, Stitziel, No, Kathiresan, S, Gabriel, S, Barrett, Jc, Lehtimäki, T, Laakso, M, Groop, L, Kaprio, J, Perola, M, Mccarthy, Mi, Boehnke, M, Altshuler DM, Lindgren CM, Hirschhorn, Jn, Metspalu, A, Freimer, Nb, Zeller, T, Jalkanen, S, Koskinen, S, Raitakari, O, Durbin, R, Macarthur, Dg, Salomaa, V, Ripatti, S, Daly, Mj, Palotie, A, Sequencing, Initiative Suomi Project

مصطلحات موضوعية: low-frequency loss-of-function variant, Cardiovascular disease, whole exome sequencing

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/PMID: 25078778; info:eu-repo/semantics/altIdentifier/wos/WOS:000339902600042; volume:10; issue:7; firstpage:1; lastpage:12; numberofpages:12; journal:PLOS GENETICS; http://hdl.handle.net/11562/868596; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84905460411; http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1004494

الاتاحة: http://hdl.handle.net/11562/868596
https://doi.org/10.1371/journal.pgen.1004494
http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1004494