المؤلفون: De Sandre-Giovannoli A, Karim Harhouri, Nicolas Lévy, Mawuse Gk, Van Maldergem L, Pierre Cau, Casey F, Yassamine Doubaj, Mejia-Baltodano G

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Mutation, Progeria, integumentary system, Point mutation, nutritional and metabolic diseases, Biology, medicine.disease, Progerin, medicine.disease_cause, Progeroid syndromes, LMNA, Exon, medicine, Cancer research, Lamin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f21267cf649bdabeb4f9cf4ee6a92326
https://doi.org/10.1101/2021.04.14.439612

المؤلفون: Mirabello, L, Zhu, B, Koster, R, Karlins, E, Dean, M, Yeager, M, Gianferante, M, Spector, LG, Morton, LM, Karyadi, D, Robison, LL, Armstrong, GT, Bhatia, S, Song, L, Pankratz, N, Pinheiro, M, Gastier-Foster, JM, Gorlick, R, de Toledo, SRC, Petrilli, AS, Patino-Garcia, A, Lecanda, F, Gutierrez-Jimeno, M, Serra, M, Hattinger, C, Picci, P, Scotlandi, K, Flanagan, AM, Tirabosco, R, Amary, MF, Kurucu, N, Ilhan, IE, Ballinger, ML, Thomas, DM, Barkauskas, DA, Mejia-Baltodano, G, Valverde, P, Hicks, BD, Wang, M, Hutchinson, AA, Tucker, M, Sampson, J, Landi, MT, Freedman, ND, Gapstur, S, Carter, B, Hoover, RN, Chanock, SJ, Savage, SA

المصدر: JAMA Oncology (2020) (In press).

Relation: https://discovery.ucl.ac.uk/id/eprint/10096599/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10096599/