Mutations in the ABC1 gene in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks-Wilson, Michel Marcil, Susanne M. Clee, Lin-Hua Zang, Kirsten Roomp, Marjel van Dam, Lu Yu, Carl Brewer, Jennifer A. Collins, Henri OF Molhuizen,, Odell Loubser, B.F. Francis Ouelette, Keith Fichter, Katherine J.D. Ashbourne-Excoffon, Christoph Wilhelm Sensen, Stephen Scherer, Stephanie Mott, Maxime Denis, Duane Martindale, Jiri Frohlich & 6 others Kenneth Morgan, Ben Koop, Simon Pimstone, John JP Kastelein, Jacques Genest Jr., Michael R. Hayden

    Research output: Contribution to journalArticleResearchpeer-review

    Original languageEnglish
    Pages (from-to)336-345
    JournalNature genetics
    Volume22
    DOIs
    Publication statusPublished - 1999

    Fields of Expertise

    • Human- & Biotechnology

    Cite this

    Brooks-Wilson, A., Marcil, M., Clee, S. M., Zang, L-H., Roomp, K., van Dam, M., ... Hayden, M. R. (1999). Mutations in the ABC1 gene in Tangier disease and familial high-density lipoprotein deficiency. Nature genetics, 22, 336-345. https://doi.org/10.1038/11905