| pubmed-article:17125728 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C0041623 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C0011350 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C1521970 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:17125728 | lifeskim:mentions | umls-concept:C1414397 | lld:lifeskim |
| pubmed-article:17125728 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:17125728 | pubmed:dateCreated | 2007-1-19 | lld:pubmed |
| pubmed-article:17125728 | pubmed:abstractText | The main clinical manifestations of amelogenesis imperfecta (AI) include alteration in the quality and quantity of enamel. AI is associated with different mutations in four genes: enamelin (ENAM), amelogenin (AMGX), kallikrein (KLK4) and enamelysin (MMP-20). Seven different mutations have been identified in the enamelin gene (ENAM). | lld:pubmed |
| pubmed-article:17125728 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17125728 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17125728 | pubmed:citationSubset | D | lld:pubmed |
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| pubmed-article:17125728 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17125728 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17125728 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:17125728 | pubmed:issn | 0003-9969 | lld:pubmed |
| pubmed-article:17125728 | pubmed:author | pubmed-author:BattelinoTade... | lld:pubmed |
| pubmed-article:17125728 | pubmed:author | pubmed-author:PetelinMilanM | lld:pubmed |
| pubmed-article:17125728 | pubmed:author | pubmed-author:PavlicAlenkaA | lld:pubmed |
| pubmed-article:17125728 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17125728 | pubmed:volume | 52 | lld:pubmed |
| pubmed-article:17125728 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17125728 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17125728 | pubmed:pagination | 209-17 | lld:pubmed |
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| pubmed-article:17125728 | pubmed:meshHeading | pubmed-meshheading:17125728... | lld:pubmed |
| pubmed-article:17125728 | pubmed:meshHeading | pubmed-meshheading:17125728... | lld:pubmed |
| pubmed-article:17125728 | pubmed:meshHeading | pubmed-meshheading:17125728... | lld:pubmed |
| pubmed-article:17125728 | pubmed:meshHeading | pubmed-meshheading:17125728... | lld:pubmed |
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| pubmed-article:17125728 | pubmed:meshHeading | pubmed-meshheading:17125728... | lld:pubmed |
| pubmed-article:17125728 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17125728 | pubmed:articleTitle | Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG. | lld:pubmed |
| pubmed-article:17125728 | pubmed:affiliation | Department of Paediatric and Preventive Dentistry, Faculty of Medicine, University of Ljubljana, Hrvatski trg 6, 1000 Ljubljana, Slovenia. alenka.pavlic@mf.uni-lj.si | lld:pubmed |
| pubmed-article:17125728 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17125728 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:10117 | entrezgene:pubmed | pubmed-article:17125728 | lld:entrezgene |
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