IGLV3-21∗01 is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling: Proceedings of the National Academy of Sciences of the United States of America

P.C. Maity, M. Bilal, M.T. Koning, M. Young, C.A.M. Van Bergen, V. Renna, A. Nicolò, M. Datta, E. Gentner-Göbel, R.S. Barendse, S.F. Somers, R.A.L. De Groen, J.S.P. Vermaat, D. Steinbrecher, C. Schneider, E. Tausch, T. Bittolo, R. Bomben, A.N. Mazzarello, G. Del PoetaW.G.M. Kroes, J.T. Van Wezel, K. Imkeller, C.E. Busse, M. Degano, T. Bakchoul, A.R. Schulz, H. Mei, P. Ghia, K. Kotta, K. Stamatopoulos, H. Wardemann, A. Zucchetto, N. Chiorazzi, V. Gattei, S. Stilgenbauer, H. Veelken, H. Jumaa

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