Source:http://linkedlifedata.com/resource/pubmed/id/18325181
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 2
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pubmed:dateCreated |
2008-3-7
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pubmed:abstractText |
Familial ligand-defective apolipoprotein B-100 (FDB) is characterized by elevated plasma concentrations of LDL-cholesterol and apolipoprotein (apo) B, normal triglyceride and HDL-cholesterol levels, the presence of tendon xanthomas, and premature coronary artery disease. FDB cannot be clinically distinguished from heterozygous LDL-receptor-defective familial hypercholesterolaemia (FH) without genetic testing.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0004-5632
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
170-6
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18325181-Apolipoproteins B,
pubmed-meshheading:18325181-Base Sequence,
pubmed-meshheading:18325181-DNA Mutational Analysis,
pubmed-meshheading:18325181-Exons,
pubmed-meshheading:18325181-Genetic Testing,
pubmed-meshheading:18325181-Humans,
pubmed-meshheading:18325181-Hyperlipoproteinemia Type II,
pubmed-meshheading:18325181-Molecular Sequence Data,
pubmed-meshheading:18325181-Mutation,
pubmed-meshheading:18325181-Sequence Analysis, DNA,
pubmed-meshheading:18325181-Temperature
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pubmed:year |
2008
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pubmed:articleTitle |
High-resolution melting analysis for detection of familial ligand-defective apolipoprotein B-100 mutations.
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pubmed:affiliation |
School of Surgery and Pathology, University of Western Australia, Perth, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Evaluation Studies
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