RT Journal Article
T1 Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.
A1 Pertesi, Maroulio
A1 Vallee, Maxime
A1 Wei, Xiaomu
A1 Revuelta, Maria V
A1 Galia, Perrine
A1 Demangel, Delphine
A1 Oliver, Javier
A1 Foll, Matthieu
A1 Chen, Siwei
A1 Perrial, Emeline
A1 Garderet, Laurent
A1 Corre, Jill
A1 Leleu, Xavier
A1 Boyle, Eileen M
A1 Decaux, Olivier
A1 Rodon, Philippe
A1 Kolb, Brigitte
A1 Slama, Borhane
A1 Mineur, Philippe
A1 Voog, Eric
A1 Le Bris, Catherine
A1 Fontan, Jean
A1 Maigre, Michel
A1 Beaumont, Marie
A1 Azais, Isabelle
A1 Sobol, Hagay
A1 Vignon, Marguerite
A1 Royer, Bruno
A1 Perrot, Aurore
A1 Fuzibet, Jean-Gabriel
A1 Dorvaux, VEronique
A1 Anglaret, Bruno
A1 Cony-Makhoul, Pascale
A1 Berthou, Christian
A1 Desquesnes, Florence
A1 Pegourie, Brigitte
A1 Leyvraz, Serge
A1 Mosser, Laurent
A1 Frenkiel, Nicole
A1 Augeul-Meunier, Karine
A1 Leduc, Isabelle
A1 Leyronnas, Cecile
A1 Voillat, Laurent
A1 Casassus, Philippe
A1 Mathiot, Claire
A1 Cheron, Nathalie
A1 Paubelle, Etienne
A1 Moreau, Philippe
A1 Bignon, Yves-Jean
A1 Joly, Bertrand
A1 Bourquard, Pascal
A1 Caillot, Denis
A1 Naman, Herve
A1 Rigaudeau, Sophie
A1 Marit, Gerald
A1 Macro, Margaret
A1 Lambrecht, Isabelle
A1 Cliquennois, Manuel
A1 Vincent, Laure
A1 Helias, Philippe
A1 Avet-Loiseau, Herve
A1 Moreno, Victor
A1 Reis, Rui Manuel
A1 Varkonyi, Judit
A1 Kruszewski, Marcin
A1 Vangsted, Annette Juul
A1 Jurczyszyn, Artur
A1 Zaucha, Jan Maciej
A1 Sainz, Juan
A1 Krawczyk-Kulis, Malgorzata
A1 Wątek, Marzena
A1 Pelosini, Matteo
A1 Iskierka-Jażdżewska, Elzbieta
A1 Grząśko, Norbert
A1 Martinez-Lopez, Joaquin
A1 Jerez, Andres
A1 Campa, Daniele
A1 Buda, Gabriele
A1 Lesueur, Fabienne
A1 Dudziński, Marek
A1 Garcia-Sanz, Ramon
A1 Nagler, Arnon
A1 Rymko, Marcin
A1 Jamroziak, Krzysztof
A1 Butrym, Aleksandra
A1 Canzian, Federico
A1 Obazee, Ofure
A1 Nilsson, Björn
A1 Klein, Robert J
A1 Lipkin, Steven M
A1 McKay, James D
A1 Dumontet, Charles
K1 Mieloma
K1 Exoma
K1 Female
K1 Germline mutation
AB Multiple myeloma (MM) is the third most common hematological malignancy, after Non-Hodgkin Lymphoma and Leukemia. MM is generally preceded by Monoclonal Gammopathy of Undetermined Significance (MGUS), and epidemiological studies have identified older age, male gender, family history, and MGUS as risk factors for developing MM.
PB Springer Nature
YR 2019
FD 2019-02-08
LK http://hdl.handle.net/10668/13806
UL http://hdl.handle.net/10668/13806
LA en
NO Pertesi M, Vallée M, Wei X, Revuelta MV, Galia P, Demangel D, et al. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma. Leukemia. 2019 Sep;33(9):2324-2330
DS RISalud
RD Apr 9, 2025