Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group

BACKGROUND: Little is known about risks associated with germline SUFU pathogenic variants (PVs) known as a cancer predisposition syndrome. METHODS: To study tumour risks, we have analysed data of a large cohort of 45 unpublished patients with a germline SUFU PV completed with 127 previously publishe...

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Detalles Bibliográficos
Autores principales: Guerrini-Rousseau, Léa, Masliah-Planchon, Julien, Waszak, Sebastian M, Alhopuro, Pia, Benusiglio, Patrick R, Bourdeaut, Franck, Brecht, Ines B, Del Baldo, Giada, Dhanda, Sandeep Kumar, Garrè, Maria Luisa, Gidding, Corrie E M, Hirsch, Steffen, Hoarau, Pauline, Jorgensen, Mette, Kratz, Christian, Lafay-Cousin, Lucie, Mastronuzzi, Angela, Pastorino, Lorenza, Pfister, Stefan M, Schroeder, Christopher, Smith, Miriam Jane, Vahteristo, Pia, Vibert, Roseline, Vilain, Catheline, Waespe, Nicolas, Winship, Ingrid M, Evans, D Gareth, Brugieres, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Cancer Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613872/
https://www.ncbi.nlm.nih.gov/pubmed/35768194
http://dx.doi.org/10.1136/jmedgenet-2021-108385

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613872/
https://www.ncbi.nlm.nih.gov/pubmed/35768194
http://dx.doi.org/10.1136/jmedgenet-2021-108385

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