Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.
(2019) Leukemia — Vol. 33, n° 9, p. 2324-2330 (2019)
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Revuelta, Maria V 
- Abstract
- (en) To the Editor, 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) [1], and epidemiological studies have identified older age, male gender, family history, and MGUS as risk factors for developing MM [...]
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Citations
Pertesi, M., Vallée, M., Wei, X., Revuelta, M. V., Galia, P., Demangel, D., Oliver, J., Foll, M., Chen, S., Perrial, E., Garderet, L., Corre, J., Leleu, X., Boyle, E. M., Decaux, O., Rodon, P., Kolb, B., Slama, B., Mineur, P., et al. (2019). Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma. Leukemia, 33(9), 2324-2330. https://doi.org/10.1038/s41375-019-0452-6 (Original work published 2019)