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

Angela Brooks‐Wilson, Michel Marcil(Xenon Pharmaceuticals (Canada)), Susanne M. Clee(University of British Columbia), Linhua Zhang(Xenon Pharmaceuticals (Canada)), Kirsten Roomp(Xenon Pharmaceuticals (Canada)), Marjel van Dam(Amsterdam UMC Location University of Amsterdam), Lu Yu(Montreal Clinical Research Institute), Carl G. Brewer(Montreal General Hospital), Jennifer A. Collins(Xenon Pharmaceuticals (Canada)), Henri O.F. Molhuizen(GGD Amsterdam), Odell Loubser(University of British Columbia), B.F. Francis Ouelette(University of British Columbia), Keith Fichter(University of British Columbia), K.J. Ashbourne-Excoffon(University of British Columbia), Christoph W. Sensen(Institute for Marine Biosciences), Stephen W. Scherer(Hospital for Sick Children), Stephanie Mott(Montreal Clinical Research Institute), Maxime Denis(Montreal Clinical Research Institute), Duane W. Martindale(University of Victoria), Jiří Fröhlich(University of British Columbia), Kenneth Morgan(Montreal General Hospital), Ben F. Koop(University of Victoria), Simon N. Pimstone(University of British Columbia), John J.P. Kastelein(Amsterdam UMC Location University of Amsterdam), Jacques Genest(Montreal Clinical Research Institute), Michael R. Hayden(University of British Columbia)
Nature Genetics
August 1, 1999
Cited by 1,708

Abstract


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