Novel ABCA1 compound variant associated with HDL cholesterol deficiency

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1587, Issue 1, 2002, Pages 60-64

  Ho Hong, Seung ^a   Rhyne, Jeffrey ^a   Zeller, Karen ^a   Miller, Michael ^a  

^a UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

Author keywords

ABCA1; HDL cholesterol deficiency; Mutation

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A1; ASPARAGINE; HIGH DENSITY LIPOPROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; PHENYLALANINE; SERINE; TYROSINE; UNCLASSIFIED DRUG;

ADULT; AGED; ALLELE; ARTICLE; CHOLESTEROL TRANSPORT; CHROMOSOME; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; DISEASE COURSE; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HETEROZYGOTE; HUMAN; LIPID BLOOD LEVEL; LIPOPROTEIN METABOLISM; MALE; MORALITY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM; TANGIER DISEASE; VASCULAR AMYLOIDOSIS;

AGED; ATP-BINDING CASSETTE TRANSPORTERS; CEREBRAL AMYLOID ANGIOPATHY; CHOLESTEROL, HDL; FATAL OUTCOME; HUMANS; MALE; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RESTRICTION MAPPING;

EID: 0037150282     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(02)00066-2     Document Type: Article

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