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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2008-10-10
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pubmed:abstractText |
Vitiligo is an autoimmune disorder that occurs with greatly increased frequency in the rare recessive autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) caused by mutations of the autoimmune regulator (AIRE) gene on chromosome 21q22.3. We have previously detected an association between alopecia areata and single nucleotide polymorphisms (SNPs) in the AIRE gene.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1365-2133
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
159
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
591-6
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pubmed:meshHeading |
pubmed-meshheading:18616774-Adult,
pubmed-meshheading:18616774-Autoimmune Diseases,
pubmed-meshheading:18616774-Case-Control Studies,
pubmed-meshheading:18616774-Female,
pubmed-meshheading:18616774-Genes, Regulator,
pubmed-meshheading:18616774-Genetic Predisposition to Disease,
pubmed-meshheading:18616774-Haplotypes,
pubmed-meshheading:18616774-Humans,
pubmed-meshheading:18616774-Male,
pubmed-meshheading:18616774-Odds Ratio,
pubmed-meshheading:18616774-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:18616774-Polymorphism, Single Nucleotide,
pubmed-meshheading:18616774-Risk Assessment,
pubmed-meshheading:18616774-Skin Diseases, Genetic,
pubmed-meshheading:18616774-Transcription Factors,
pubmed-meshheading:18616774-Vitiligo
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pubmed:year |
2008
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pubmed:articleTitle |
The autoimmune regulator gene (AIRE) is strongly associated with vitiligo.
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pubmed:affiliation |
Division of Genomic Medicine, University of Sheffield, Sheffield S10 2RX, UK. r.taziahnini@sheffield.ac.uk
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pubmed:publicationType |
Journal Article
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