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Common variants in FOXP1 are associated with generalized vitiligo

Jin, Y; Birlea, SA; Fain, PR; Mailloux, CM; Riccardi, SL; Gowan, K; Holland, PJ; Bennett, DC; Wallace, MR; McCormack, WT; et al. Jin, Y; Birlea, SA; Fain, PR; Mailloux, CM; Riccardi, SL; Gowan, K; Holland, PJ; Bennett, DC; Wallace, MR; McCormack, WT; Kemp, EH; Gawkrodger, DJ; Weetman, AP; Picardo, M; Leone, G; Taïeb, A; Jouary, T; Ezzedine, K; van Geel, N; Lambert, J; Overbeck, A; Spritz, RA (2010) Common variants in FOXP1 are associated with generalized vitiligo. NATURE GENETICS, 42 (7). 576 - 578 (3). ISSN 1061-4036 https://doi.org/10.1038/ng.602
SGUL Authors: Bennett, Dorothy Catherine

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Item Type: Article
Additional Information: PubMed ID: 20526340
Keywords: Chromosomes,Human,Pair 3, Family Health, Forkhead Transcription Factors, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, genetics, Genome-Wide Association Study, Genotype, Humans, Linkage Disequilibrium, Polymorphism,Single Nucleotide, Repressor Proteins, Vitiligo, Chromosomes, Human, Pair 3, Family Health, Forkhead Transcription Factors, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Genotype, Humans, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Repressor Proteins, Vitiligo, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, GENOME-WIDE ASSOCIATION, ESSENTIAL TRANSCRIPTIONAL REGULATOR, T-CELLS, SUSCEPTIBILITY LOCI, AUTOIMMUNITY, GENETICS, DISEASES, IDDM8
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: NATURE GENETICS
ISSN: 1061-4036
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Dates:
DateEvent
1 July 2010Published
Web of Science ID: WOS:000279242400009
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URI: https://openaccess.sgul.ac.uk/id/eprint/1936
Publisher's version: https://doi.org/10.1038/ng.602

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