| pubmed-article:20222933 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0406811 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C1416742 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0183683 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C0220922 | lld:lifeskim |
| pubmed-article:20222933 | lifeskim:mentions | umls-concept:C1512571 | lld:lifeskim |
| pubmed-article:20222933 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:20222933 | pubmed:dateCreated | 2010-7-21 | lld:pubmed |
| pubmed-article:20222933 | pubmed:abstractText | Galli-Galli disease (GGD) is a rare genodermatosis. Its clinical presentation is identical to that of Dowling-Degos disease (DDD), but the presence of the histopathological feature of acantholysis in GGD is thought to distinguish the two disorders. Mutations in the keratin 5 gene (KRT5) have been identified in the majority of patients with DDD and in a small number of patients with GGD. | lld:pubmed |
| pubmed-article:20222933 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20222933 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20222933 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20222933 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20222933 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20222933 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20222933 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:20222933 | pubmed:issn | 1365-2133 | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:WenzelJJ | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:RuzickaTT | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:LVOVAT NTN | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:NöthenM MMM | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:WattelCC | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:Braun-FalcoMM | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:HannekenSS | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:BetzR CRC | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:El... | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:EigelshovenSS | lld:pubmed |
| pubmed-article:20222933 | pubmed:author | pubmed-author:PasternackS... | lld:pubmed |
| pubmed-article:20222933 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20222933 | pubmed:volume | 163 | lld:pubmed |
| pubmed-article:20222933 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20222933 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20222933 | pubmed:pagination | 197-200 | lld:pubmed |
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| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
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| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
| pubmed-article:20222933 | pubmed:meshHeading | pubmed-meshheading:20222933... | lld:pubmed |
| pubmed-article:20222933 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20222933 | pubmed:articleTitle | Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. | lld:pubmed |
| pubmed-article:20222933 | pubmed:affiliation | Department of Dermatology, University Hospital Düsseldorf, Moorenstrasse 5, 40225 Düsseldorf, Germany. Hanneken@med.uni-duesseldorf.de | lld:pubmed |
| pubmed-article:20222933 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20222933 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:3852 | entrezgene:pubmed | pubmed-article:20222933 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20222933 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:20222933 | lld:pubmed |
