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pro vyhledávání: '"Martina Müller-Nurasyid"'
Autor:
Matthias Simon, Marta Rossetto, S. J. Hepworth, Marc Sanson, Richard S. Houlston, Marianne Labussière, Victor Enciso-Mora, Peter Broderick, Yuexin Liu, Georgina Armstrong, Martina Müller-Nurasyid, Agusti Alentorn, Fay J. Hosking, Minouk J. Schoemaker, Diana Zelenika, Jean Yves Delattre, Stefan Schreiber, Ahmed Idbaih, Ching C. Lau, Susanne Moebus, Sanjay Shete, Pietro Ciccarino, Lewin Eisele, Johannes Schramm, Anthony J. Swerdlow, Khê Hoang-Xuan, Mark Lathrop, Andre Franke, Konstantin Strauch, Yannick Marie, A. L. Di Stefano, Konstantinos Gousias, Melissa L. Bondy
Publikováno v:
Br. J. Cancer 108, 2178-2185 (2013)
British Journal of Cancer
British Journal of Cancer
Background: Most of the heritable risk of glioma is presently unaccounted for by mutations in known genes. In addition to rare inactivating germline mutations in TP53 causing glioma in the context of the Li-Fraumeni syndrome, polymorphic variation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::496c558994355b9c0d7f8efd4dcf6331
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=25513
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=25513