| Title | Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma. |
| Publication Type | Journal Article |
| Year of Publication | 2019 |
| Authors | Pertesi, M, Vallée, M, Wei, X, Revuelta, MV, Galia, P, Demangel, D, Oliver, J, Foll, M, Chen, S, Perrial, E, Garderet, L, Corre, J, Leleu, X, Boyle, EM, Decaux, O, Rodon, P, Kolb, B, Slama, B, Mineur, P, Voog, E, Le Bris, C, Fontan, J, Maigre, M, Beaumont, M, Azais, I, Sobol, H, Vignon, M, Royer, B, Perrot, A, Fuzibet, J-G, Dorvaux, V, Anglaret, B, Cony-Makhoul, P, Berthou, C, Desquesnes, F, Pegourie, B, Leyvraz, S, Mosser, L, Frenkiel, N, Augeul-Meunier, K, Leduc, I, Leyronnas, C, Voillat, L, Casassus, P, Mathiot, C, Cheron, N, Paubelle, E, Moreau, P, Bignon, Y-J, Joly, B, Bourquard, P, Caillot, D, Naman, H, Rigaudeau, S, Marit, G, Macro, M, Lambrecht, I, Cliquennois, M, Vincent, L, Helias, P, Avet-Loiseau, H, Moreno, V, Reis, RManuel, Varkonyi, J, Kruszewski, M, Vangsted, AJuul, Jurczyszyn, A, Zaucha, JMaciej, Sainz, J, Krawczyk-Kulis, M, Wątek, M, Pelosini, M, Iskierka-Jażdżewska, E, Grząśko, N, Martinez-Lopez, J, Jerez, A, Campa, D, Buda, G, Lesueur, F, Dudziński, M, García-Sanz, R, Nagler, A, Rymko, M, Jamroziak, K, Butrym, A, Canzian, F, Obazee, O, Nilsson, B, Klein, RJ, Lipkin, SM, McKay, JD, Dumontet, C |
| Journal | Leukemia |
| Volume | 33 |
| Issue | 9 |
| Pagination | 2324-2330 |
| Date Published | 2019 09 |
| ISSN | 1476-5551 |
| Keywords | Exome, Exosome Multienzyme Ribonuclease Complex, Female, Genetic Predisposition to Disease, Germ-Line Mutation, Humans, Multiple Myeloma, Pedigree, Whole Exome Sequencing |
| DOI | 10.1038/s41375-019-0452-6 |
| Alternate Journal | Leukemia |
| PubMed ID | 30967618 |
| PubMed Central ID | PMC6756025 |
| Grant List | R01 CA167824 / CA / NCI NIH HHS / United States
S10 OD018522 / OD / NIH HHS / United States |
