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
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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 |
Related URLs: |
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Dates: |
Date | Event |
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1 July 2010 | Published |
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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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