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| pubmed-article:18349089 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:18349089 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:18349089 | pubmed:dateCreated | 2008-3-19 | lld:pubmed |
| pubmed-article:18349089 | pubmed:abstractText | Mutations in the low-density lipoprotein receptor-related protein 5 (LRP5) gene cause rare syndromes characterized by altered bone mineral density (BMD). More common LRP5 variants may affect osteoporosis risk in the general population. | lld:pubmed |
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| pubmed-article:18349089 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18349089 | pubmed:status | MEDLINE | lld:pubmed |
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| pubmed-article:18349089 | pubmed:issn | 1538-3598 | lld:pubmed |
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| pubmed-article:18349089 | pubmed:pagination | 1277-90 | lld:pubmed |
| pubmed-article:18349089 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:18349089 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18349089 | pubmed:articleTitle | Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis. | lld:pubmed |
| pubmed-article:18349089 | pubmed:affiliation | Department of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands. | lld:pubmed |
| pubmed-article:18349089 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18349089 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18349089 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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