Common variants in FOXP1 are associated with generalized vitiligo

Nature Genetics

Volumn 42, Issue 7, 2010, Pages 576-578

  Jin, Ying ^a,b   Birlea, Stanca A ^a   Fain, Pamela R ^a,b   Mailloux, Christina M ^a   Riccardi, Sheri L ^a   Gowan, Katherine ^a   Holland, Paulene J ^a   Bennett, Dorothy C ^c   Wallace, Margaret R ^d   McCormack, Wayne T ^d   Kemp, E Helen ^e   Gawkrodger, David J ^f   Weetman, Anthony P ^e   Picardo, Mauro ^g   Leone, Giovanni ^g   Taĩeb, Alain ^h   Jouary, Thomas ^h   Ezzedine, Khaled ^h   Van Geel, Nanny ⁱ   Lambert, Jo ⁱ   Overbeck, Andreas ^j   Spritz, Richard A ^a,b   more..

^a UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

^b Children's Hospital Colorado   (United States)

^c ST GEORGE S HOSPITAL   (United Kingdom)

^d UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^e UNIVERSITY OF SHEFFIELD   (United Kingdom)

^f ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

^g SAN GALLICANO DERMATOLOGICAL INSTITUTE   (Italy)

^h HÔPITAL SAINT ANDRÉ   (France)

ⁱ GHENT UNIVERSITY HOSPITAL   (Belgium)

^j Lumiderm   (Spain)

more..

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXP1; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 3P; CHROMOSOME 6Q; CONTROLLED STUDY; FOXP1 GENE; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; 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;

EID: 77954143391     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.602     Document Type: Article

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