Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

Translated title of the contribution: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

L.A. Lange, Y. Hu, H. Zhang, C. Xue, E.M. Schmidt, Z.Z. Tang, C. Bizon, E.M. Lange, J.D. Smith, E.H. Turner, G. Jun, H.M. Kang, G. Peloso, P. Auer, K.P. Li, J. Flannick, J. Zhang, C. Fuchsberger, K. Gaulton, C. LindgrenA. Locke, A. Manning, X. Sim, M.A. Rivas, O.L. Holmen, [No Value] et al, P.I.W. de Bakker, X NHLBI Grand Opportunity Exome Sequencing Project, C.J. Willer

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionWhole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
Original languageUndefined/Unknown
Pages (from-to)233-245
Number of pages13
JournalAmerican Journal of Human Genetics
Volume94
Issue number2
Publication statusPublished - 2014

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde(GENK)
  • Medical sciences
  • Bescherming en bevordering van de menselijke gezondheid

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