Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux

Michel Marcil, Angela Brooks-Wilson, Susanne M. Clee, Kirsten Roomp, Lin-Hua Zang, Lu Yu, Jennifer A. Collins, Marjel van Dam, Henri OF Molhuizen,, Odell Loubster, BF Francis Ouellette, Christoph Wilhelm Sensen, Keith Fichter, Stephanie Mott, Maxime Denis, Betsie Boucher, Simon Pimstone, Jacques Genest Jr., John JP Kastelein, Michael R. Hayden

    Research output: Contribution to journalArticleResearchpeer-review

    Original languageEnglish
    Pages (from-to)1341-1346
    JournalThe Lancet
    Volume354
    Issue number9187
    DOIs
    Publication statusPublished - 1999

    Fields of Expertise

    • Human- & Biotechnology

    Cite this

    Marcil, M., Brooks-Wilson, A., Clee, S. M., Roomp, K., Zang, L-H., Yu, L., ... Hayden, M. R. (1999). Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. The Lancet, 354(9187), 1341-1346. https://doi.org/10.1016/S0140-6736(99)07026-9

    Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. / Marcil, Michel; Brooks-Wilson, Angela; Clee, Susanne M.; Roomp, Kirsten; Zang, Lin-Hua; Yu, Lu; Collins, Jennifer A.; van Dam, Marjel; Molhuizen, Henri OF; Loubster, Odell; Ouellette, BF Francis; Sensen, Christoph Wilhelm; Fichter, Keith; Mott, Stephanie; Denis, Maxime; Boucher, Betsie; Pimstone, Simon; Genest Jr., Jacques; Kastelein, John JP; Hayden, Michael R.

    In: The Lancet, Vol. 354, No. 9187, 1999, p. 1341-1346.

    Research output: Contribution to journalArticleResearchpeer-review

    Marcil, M, Brooks-Wilson, A, Clee, SM, Roomp, K, Zang, L-H, Yu, L, Collins, JA, van Dam, M, Molhuizen, HOF, Loubster, O, Ouellette, BFF, Sensen, CW, Fichter, K, Mott, S, Denis, M, Boucher, B, Pimstone, S, Genest Jr., J, Kastelein, JJP & Hayden, MR 1999, 'Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux' The Lancet, vol. 354, no. 9187, pp. 1341-1346. https://doi.org/10.1016/S0140-6736(99)07026-9
    Marcil M, Brooks-Wilson A, Clee SM, Roomp K, Zang L-H, Yu L et al. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. The Lancet. 1999;354(9187):1341-1346. https://doi.org/10.1016/S0140-6736(99)07026-9
    Marcil, Michel ; Brooks-Wilson, Angela ; Clee, Susanne M. ; Roomp, Kirsten ; Zang, Lin-Hua ; Yu, Lu ; Collins, Jennifer A. ; van Dam, Marjel ; Molhuizen, Henri OF ; Loubster, Odell ; Ouellette, BF Francis ; Sensen, Christoph Wilhelm ; Fichter, Keith ; Mott, Stephanie ; Denis, Maxime ; Boucher, Betsie ; Pimstone, Simon ; Genest Jr., Jacques ; Kastelein, John JP ; Hayden, Michael R. / Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. In: The Lancet. 1999 ; Vol. 354, No. 9187. pp. 1341-1346.
    @article{17be8f12dccf45218274f9a0df736ee3,
    title = "Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux",
    author = "Michel Marcil and Angela Brooks-Wilson and Clee, {Susanne M.} and Kirsten Roomp and Lin-Hua Zang and Lu Yu and Collins, {Jennifer A.} and {van Dam}, Marjel and Molhuizen,, {Henri OF} and Odell Loubster and Ouellette, {BF Francis} and Sensen, {Christoph Wilhelm} and Keith Fichter and Stephanie Mott and Maxime Denis and Betsie Boucher and Simon Pimstone and {Genest Jr.}, Jacques and Kastelein, {John JP} and Hayden, {Michael R.}",
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    T1 - Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux

    AU - Marcil, Michel

    AU - Brooks-Wilson, Angela

    AU - Clee, Susanne M.

    AU - Roomp, Kirsten

    AU - Zang, Lin-Hua

    AU - Yu, Lu

    AU - Collins, Jennifer A.

    AU - van Dam, Marjel

    AU - Molhuizen,, Henri OF

    AU - Loubster, Odell

    AU - Ouellette, BF Francis

    AU - Sensen, Christoph Wilhelm

    AU - Fichter, Keith

    AU - Mott, Stephanie

    AU - Denis, Maxime

    AU - Boucher, Betsie

    AU - Pimstone, Simon

    AU - Genest Jr., Jacques

    AU - Kastelein, John JP

    AU - Hayden, Michael R.

    PY - 1999

    Y1 - 1999

    U2 - 10.1016/S0140-6736(99)07026-9

    DO - 10.1016/S0140-6736(99)07026-9

    M3 - Article

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    SP - 1341

    EP - 1346

    JO - The Lancet

    JF - The Lancet

    SN - 0140-6736

    IS - 9187

    ER -