MBCL-39. MEDULLOBLASTOMA IN PATIENTS WITH GORLIN SYNDROME: RESULTS FROM THE HIT STUDY GROUP

Gorlin syndrome is an autosomal dominant inherited cancer predisposition syndrome characterized by basal cell carcinomas, odontogenic keratocysts, skeletal and multiple other anomalies, and medulloblastoma (MB). Most patients harbor a heterozygous germline mutation in PTCH1 or SUFU, genes that play...

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Publicado en:Neuro Oncol
Main Authors: Meissner, Barbara, Mynarek, Martin, Ole Juhnke, B, von Hoff, Katja, Pietsch, Torsten, Kortmann, Rolf D, Warmuth-Metz, Monika, Bison, Brigitte, Rutkowski, Stefan
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2018
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6012922/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noy059.435
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