dc.contributor.author | Marcil, M | fr_FR |
dc.contributor.author | Brooks-Wilson, A | fr_FR |
dc.contributor.author | Kastelein, J | fr_FR |
dc.contributor.author | Hayden, M | fr_FR |
dc.contributor.author | Genest, J Jr | fr_FR |
dc.date.accessioned | 2012-08-30T12:32:31Z | |
dc.date.available | 2012-08-30T12:32:31Z | |
dc.date.issued | 2000 | fr_FR |
dc.identifier.citation | Marcil, M ; Brooks-Wilson, A ; Kastelein, J ; Hayden, M ; Genest, J Jr, Mutations du gène de l'ATP binding cassette-1 (ABC1) dans la maladie de Tangier et la déficience familiale en HDL., Med Sci (Paris), 2000, Vol. 16, N° 3; p.421-3 | fr_FR |
dc.identifier.issn | 1958-5381 | fr_FR |
dc.identifier.uri | http://hdl.handle.net/10608/1664 | |
dc.language.iso | fr | fr_FR |
dc.publisher | Masson, Paris | fr_FR |
dc.rights | Article en libre accès | fr |
dc.rights | Médecine/Sciences - Inserm - SRMS | fr |
dc.source | M/S. Médecine sciences [revue papier, ISSN : 0767-0974], 2000, Vol. 16, N° 3; p.421-3 | fr_FR |
dc.title | Mutations du gène de l'ATP binding cassette-1 (ABC1) dans la maladie de Tangier et la déficience familiale en HDL. | fr |
dc.title.alternative | Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. | fr_FR |
dc.type | Article | fr_FR |
dc.contributor.affiliation | M. Marcil, Lab. genetique cardio-vasculaire, Inst. recherches cliniques Montreal, 110 Avenue des Pins Ouest, Montreal, Que. H2 1R7; Canada | - |
dc.identifier.doi | 10.4267/10608/1664 | |