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

Nature Genetics

Volumn 22, Issue 4, 1999, Pages 336-345

  Brooks Wilson, Angela ^a   Marcil, Michel ^a   Clee, Susanne M ^b   Zhang, Lin Hua ^a   Roomp, Kirsten ^a   Van Dam, Marjel ^c   Yu, Lu ^d   Brewer, Carl ^e   Collins, Jennifer A ^a   Molhuizen, Henri O F ^c   Loubser, Odell ^b   Ouelette, B F Francis ^b   Fichter, Keith ^b   Ashbourne Excoffon, Katherine J D ^b   Sensen, Christoph W ^a   Scherer, Stephen ^f   Mott, Stephanie ^d   Denis, Maxime ^d   Martindale, Duane ^f   Frohlich, Jiri ^b   Morgan, Kenneth ^e   Koop, Ben ^f   Pimstone, Simon ^b   Kastelein, John J P ^c   Genest Jr , Jacques ^d   Hayden, Michael R ^b   more..

^a NATIONAL RESEARCH COUNCIL CANADA   (Canada)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

^e MONTREAL GENERAL HOSPITAL   (Canada)

^f NRC ^*

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; REGULATOR PROTEIN;

ALLELE; ARTICLE; CASE REPORT; CHOLESTEROL TRANSPORT; CHROMOSOME 9Q; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENETIC RECOMBINATION; HUMAN; LIPID BLOOD LEVEL; MALE; MEIOSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TANGIER DISEASE;

ADULT; AMINO ACID SEQUENCE; ATP-BINDING CASSETTE TRANSPORTERS; BASE SEQUENCE; CHOLESTEROL, HDL; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC MARKERS; GLYCOPROTEINS; HUMANS; LINKAGE (GENETICS); MALE; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHYSICAL CHROMOSOME MAPPING; SEQUENCE HOMOLOGY, AMINO ACID; TANGIER DISEASE;

EID: 0032813808     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/11905     Document Type: Article

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