RARE-21. CANCER SPECTRUM IN GERMLINE SUFU MUTATION CARRIERS: A COLLABORATIVE PROJECT OF THE SIOPE HOST GENOME WORKING GROUP

BACKGROUND: Little is known about cancer risk associated with pathogenic germline SUFU variants. METHODS: Data of all previously published and 25 still unpublished patients with a pathogenic germline SUFU mutation were compiled. RESULTS: 124 patients in 67 families were identified, most of them asce...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neuro Oncol
Prif Awduron: Guerrini-Rousseau, Léa, Waszak, Sebastian, Bourdeaut, Franck, Delattre, Olivier, Dikow, Nicola, Dufour, Christelle, Gajjar, Amar, Grill, Jacques, Hirsch, Steffen, Hopman, Saskia, Jones, David, Jongmans, Majoline, Korshunov, Andrey, Kratz, Christian, Lafay-Cousin, Lucie, Masliah, Julien, Milde, Till, Northcott, Paul, Pajtler, Kristian, Pfister, Stefan, Puget, Stéphanie, Collonge, Marie Agnès Rame, Robinson, Giles, Sariban, Eric, Sevenet, Nicolas, Smith, Miriam, Sturm, Dominik, Zattara, Hélène, Varlet, Pascale, Evans, Gareth, Brugières, Laurence
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2020
Pynciau:
Craniopharyngioma and Rare Tumors
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715142/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.732
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