| pubmed-article:20683201 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20683201 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
| pubmed-article:20683201 | lifeskim:mentions | umls-concept:C0008370 | lld:lifeskim |
| pubmed-article:20683201 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:20683201 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:20683201 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:20683201 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:20683201 | pubmed:dateCreated | 2010-9-27 | lld:pubmed |
| pubmed-article:20683201 | pubmed:abstractText | The discovery of genetic mutations in children with inherited syndromes of intrahepatic cholestasis allows for diagnostic specificity despite similar clinical phenotypes. Here, we aimed to determine whether mutation screening of target genes could assign a molecular diagnosis in children with idiopathic cholestasis. | lld:pubmed |
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| pubmed-article:20683201 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20683201 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20683201 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20683201 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:20683201 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20683201 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:20683201 | pubmed:issn | 1536-4801 | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:EliaJJJr | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:BezerraJorge... | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:MiethkeAlexan... | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:MatteUrsulaU | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:KejianZhangZ | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:MouryaReenaR | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:MoyerKatieK | lld:pubmed |
| pubmed-article:20683201 | pubmed:author | pubmed-author:KauffmannGreg... | lld:pubmed |
| pubmed-article:20683201 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20683201 | pubmed:volume | 51 | lld:pubmed |
| pubmed-article:20683201 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20683201 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20683201 | pubmed:pagination | 488-93 | lld:pubmed |
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| pubmed-article:20683201 | pubmed:meshHeading | pubmed-meshheading:20683201... | lld:pubmed |
| pubmed-article:20683201 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20683201 | pubmed:articleTitle | Analysis of gene mutations in children with cholestasis of undefined etiology. | lld:pubmed |
| pubmed-article:20683201 | pubmed:affiliation | Hospital de Clinicas de Porto Alegre, Porto Alegre, RS, Brazil. | lld:pubmed |
| pubmed-article:20683201 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20683201 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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