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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. Lindgren
  • A. 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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