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Volumn 58, Issue 2, 1996, Pages 281-291
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A 10-bp deletion in the apolipoprotein E gene causing apolipoprotein E deficiency and severe type HI hyperlipoproteinemia
a,d
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID;
APOLIPOPROTEIN E;
CHOLESTEROL;
DNA;
FENOFIBRATE;
HIGH DENSITY LIPOPROTEIN CHOLESTEROL;
LIPID;
LIPOPROTEIN;
LOW DENSITY LIPOPROTEIN CHOLESTEROL;
NUCLEOTIDE;
TRIACYLGLYCEROL;
VERY LOW DENSITY LIPOPROTEIN CHOLESTEROL;
ADOLESCENT;
ADULT;
AGED;
AMINO ACID SEQUENCE;
ARTICLE;
CHILD;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DENSITY GRADIENT CENTRIFUGATION;
EXON;
FEMALE;
GENE;
GENE DELETION;
HETEROZYGOTE;
HOMOZYGOTE;
HUMAN;
HYPERLIPOPROTEINEMIA TYPE 3;
IMMUNOBLOTTING;
MALE;
MUTATION;
PEDIGREE;
PHENOTYPE;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
STOP CODON;
XANTHOMA;
ADOLESCENT;
ADULT;
AGED;
AMINO ACID SEQUENCE;
APOLIPOPROTEINS E;
BASE SEQUENCE;
CHILD;
CHOLESTEROL;
DNA PRIMERS;
FEMALE;
FRAMESHIFT MUTATION;
HETEROZYGOTE;
HUMANS;
HYPERLIPOPROTEINEMIAS;
LIPOPROTEINS;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
PEDIGREE;
SEQUENCE ANALYSIS;
SEQUENCE DELETION;
XANTHOMATOSIS;
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EID: 0030045804
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (30)
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References (5)
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