| pubmed-article:19478477 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0019425 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0008058 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0024137 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0678226 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C1336670 | lld:lifeskim |
| pubmed-article:19478477 | lifeskim:mentions | umls-concept:C0376315 | lld:lifeskim |
| pubmed-article:19478477 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:19478477 | pubmed:dateCreated | 2009-8-26 | lld:pubmed |
| pubmed-article:19478477 | pubmed:abstractText | Chilblain lupus erythematosus is a rare form of cutaneous lupus erythematosus characterized by bluish red infiltrates in acral locations of the body mostly affecting middle-aged women. We recently described a familial form of chilblain lupus manifesting in early childhood caused by a heterozygous mutation in the TREX1 gene, which encodes a 3'-5' DNA exonuclease. Thus, familial chilblain lupus represents the first monogenic form of cutaneous lupus erythematosus. Here we describe the unusual clinical course of this newly defined genodermatosis in an 18-year-old female member of the family in which familial chilblain lupus was originally described. | lld:pubmed |
| pubmed-article:19478477 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19478477 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19478477 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19478477 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19478477 | pubmed:issn | 1421-9832 | lld:pubmed |
| pubmed-article:19478477 | pubmed:author | pubmed-author:SteinAA | lld:pubmed |
| pubmed-article:19478477 | pubmed:author | pubmed-author:MeurerMM | lld:pubmed |
| pubmed-article:19478477 | pubmed:author | pubmed-author:GüntherCC | lld:pubmed |
| pubmed-article:19478477 | pubmed:author | pubmed-author:Lee-KirschM... | lld:pubmed |
| pubmed-article:19478477 | pubmed:author | pubmed-author:ViehwegAA | lld:pubmed |
| pubmed-article:19478477 | pubmed:copyrightInfo | Copyright 2009 S. Karger AG, Basel. | lld:pubmed |
| pubmed-article:19478477 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19478477 | pubmed:volume | 219 | lld:pubmed |
| pubmed-article:19478477 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19478477 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19478477 | pubmed:pagination | 162-6 | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:meshHeading | pubmed-meshheading:19478477... | lld:pubmed |
| pubmed-article:19478477 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19478477 | pubmed:articleTitle | Familial chilblain lupus--a monogenic form of cutaneous lupus erythematosus due to a heterozygous mutation in TREX1. | lld:pubmed |
| pubmed-article:19478477 | pubmed:affiliation | University Hospital for Dermatology, Technical University Dresden, Dresden, Germany. claudia.guenther@uniklinikum-dresden.de | lld:pubmed |
| pubmed-article:19478477 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19478477 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:19478477 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:11277 | entrezgene:pubmed | pubmed-article:19478477 | lld:entrezgene |
