Reference : Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
Scientific journals : Article
Scientific journals : Article
http://hdl.handle.net/10993/3318
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
English
Brooks-Wilson, A. [> >]
Marcil, M. [> >]
Clee, S. M. [> >]
Zhang, L. H. [> >]
Rump, Kirsten mailto [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. [> >]
Aug-1999
Nature Genetics
Nature Publishing Group
22
4
336-45
Yes (verified by ORBilu)
1061-4036
1546-1718
New York
NY
[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
http://hdl.handle.net/10993/3318
10.1038/11905

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