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Article (Scientific journals)
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
Brooks-Wilson, A.; Marcil, M.; Clee, S. M. et al.
1999In Nature Genetics, 22 (4), p. 336-45
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Keywords :
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
Disciplines :
UNKNOWN KEY #A01
Identifiers :
UNILU:UL-ARTICLE-2010-706
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.
More authors (16 more) Less
Language :
English
Title :
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
Publication date :
August 1999
Journal title :
Nature Genetics
ISSN :
1546-1718
Publisher :
Nature Publishing Group, New York, United States - New York
Volume :
22
Issue :
4
Pages :
336-45
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 03 July 2013

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