Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up

J.E. Martin, J.C. Broen, F.D. Carmona, M. Teruel, C.P. Simeon, M.C. Vonk, R. van't Slot, L. Rodriguez-Rodriguez, E. Vicente, V. Fonollosa, N. Ortego-Centeno, M.A. Gonzalez-Gay, F.J. Garcia-Hernandez, P.G. de la Pena, P. Carreira, A.E. Voskuyl, A.J. Schuerwegh, P.L.C.M. van Riel, A. Kreuter, T. WitteG. Riemekasten, P. Airo, R. Scorza, C. Lunardi, N. Hunzelmann, J.H.W. Distler, L. Beretta, J. van Laar, M.M. Chee, J. Worthington, A. Herrick, C. Denton, F.K. Tan, F.C. Arnett, S. Assassi, C. Fonseca, M.D. Mayes, T.R.D.J. Radstake, B.P.C. Koeleman, J. Martin

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)2825-2835
JournalHuman Molecular Genetics
Volume21
Issue number12
DOIs
Publication statusPublished - 2012

Cite this

Martin, J. E., Broen, J. C., Carmona, F. D., Teruel, M., Simeon, C. P., Vonk, M. C., ... Martin, J. (2012). Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up. Human Molecular Genetics, 21(12), 2825-2835. https://doi.org/10.1093/hmg/dds099