Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R/IL12RB2 regions associated with Behçet's disease

Detalles Bibliográficos
Autores principales: Remmers, Elaine F., Cosan, Fulya, Kirino, Yohei, Ombrello, Michael J., Abaci, Neslihan, Satorius, Colleen, Le, Julie M., Yang, Barbara, Korman, Benjamin D., Cakiris, Aris, Aglar, Oznur, Emrence, Zeliha, Azakli, Hulya, Ustek, Duran, Tugal-Tutkun, Ilknur, Akman-Demir, Gulsen, Chen, Wei, Amos, Christopher I., Dizon, Michael B., Kose, Afet Akdag, Azizlerli, Gulsevim, Erer, Burak, Brand, Oliver J., Kaklamani, Virginia G., Kaklamanis, Phaedon, Ben-Chetrit, Eldad, Stanford, Miles, Fortune, Farida, Ghabra, Marwen, Ollier, William E. R., Cho, Young-Hun, Bang, Dongsik, O'Shea, John, Wallace, Graham R., Gadina, Massimo, Kastner, Daniel L., Gül, Ahmet
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923807/
https://www.ncbi.nlm.nih.gov/pubmed/20622878
http://dx.doi.org/10.1038/ng.625

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923807/
https://www.ncbi.nlm.nih.gov/pubmed/20622878
http://dx.doi.org/10.1038/ng.625

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