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

Brooks-Wilson, A.; Marcil, M.; Clee, S. M.; Zhang, L. H.; RUMP, Kirsten; 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.

doi:10.1038/11905

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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.

1999 • In Nature Genetics, 22 (4), p. 336-45

Peer Reviewed verified by ORBi

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https://hdl.handle.net/10993/3318

DOI
10.1038/11905

PubMed
10431236

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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.

More authors (16 more)

Language :

English

Title :

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

Publication date :

August 1999

Journal title :

Nature Genetics

ISSN :

1061-4036

eISSN :

1546-1718

Publisher :

Nature Publishing Group, New York, United States - New York

Volume :

Issue :

Pages :

336-45

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBilu :

since 03 July 2013

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