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

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


	Document type :	Scientific journals : Article
	Discipline(s) :	Scientific journals : Article
	To cite this reference:	http://hdl.handle.net/10993/3318

Title :	Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
Language :	English
Author, co-author :	Brooks-Wilson, A. [> >]
	Marcil, M. [> >]
	Clee, S. M. [> >]
	Zhang, L. H. [> >]
	Rump, Kirsten [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > >]
	van Dam, M. [> >]
	Yu, L. [> >]
	Brewer, C. [> >]
	Collins, J. A. [> >]
	Molhuizen, H. O. [> >]
	Loubser, O. [> >]
	Ouelette, B. F. [> >]
	Fichter, K. [> >]
	Ashbourne-Excoffon, K. J. [> >]
	Sensen, C. W. [> >]
	Scherer, S. [> >]
	Mott, S. [> >]
	Denis, M. [> >]
	Martindale, D. [> >]
	Frohlich, J. [> >]
	Morgan, K. [> >]
	Koop, B. [> >]
	Pimstone, S. [> >]
	Kastelein, J. J. [> >]
	Genest Jr., J. [> >]
	Hayden, M. R. [> >]
Publication date :	Aug-1999
Journal title :	Nature Genetics
Publisher :	Nature Publishing Group
Volume :	22
Issue/season :	4
Pages :	336-45
Peer reviewed :	Yes (verified by ORBi^lu)
ISSN :	1061-4036
e-ISSN :	1546-1718
City :	New York
Country :	NY
Keywords :	[en] ATP-Binding Cassette Transporters/ genetics/metabolism ; Adult ; Amino Acid Sequence ; Base Sequence ; Cholesterol, HDL/ deficiency ; Chromosomes, Human, Pair 9 ; Female ; Genetic Markers ; Glycoproteins/ genetics/metabolism ; Humans ; Linkage (Genetics) ; Male ; Models, Genetic ; Molecular Sequence Data ; Mutation ; Pedigree ; Physical Chromosome Mapping ; Sequence Homology, Amino Acid ; Tangier Disease/ genetics
Permalink :	http://hdl.handle.net/10993/3318
DOI :	10.1038/11905

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