| pubmed-article:18714375 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0301630 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0445223 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0547047 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C1552599 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
| pubmed-article:18714375 | lifeskim:mentions | umls-concept:C1704787 | lld:lifeskim |
| pubmed-article:18714375 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:18714375 | pubmed:dateCreated | 2008-8-20 | lld:pubmed |
| pubmed-article:18714375 | pubmed:abstractText | Rare mutations of the low-density lipoprotein receptor gene (LDLR) cause familial hypercholesterolemia, which increases the risk for coronary artery disease (CAD). Less is known about the implications of common genetic variation in the LDLR gene regarding the variability of cholesterol levels and risk of CAD. | lld:pubmed |
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| pubmed-article:18714375 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18714375 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18714375 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18714375 | pubmed:issn | 1932-6203 | lld:pubmed |
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| pubmed-article:18714375 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18714375 | pubmed:volume | 3 | lld:pubmed |
| pubmed-article:18714375 | pubmed:owner | NLM | lld:pubmed |
