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. Witte, G. 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
  • Human Molecular Genetics, March 2012, Oxford University Press (OUP)
  • DOI: 10.1093/hmg/dds099

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http://dx.doi.org/10.1093/hmg/dds099

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