PDCT-02. UNIQUE CONCURRENT ASSOCIATION OF SOMATIC AND GERMLINE NF1 MUTATIONS WITH GERMLINE MISMATCH REPAIR MUTATIONS IN PEDIATRIC GLIOBLASTOMA MULTIFORME

INTRODUCTION: We report the first known cases of pediatric glioblastoma (GBM) with prior clinical NF1 diagnoses, one with concurrent germline Lynch syndrome (LS) and NF1, and the other with somatic NF1 mutation and germline constitutional mismatch repair deficiency (CMMRD). Pediatric GBMs in NF1 are...

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發表在:Neuro Oncol
Main Authors: Baig, Muhammed, Fuller, Greg, Gupta, Sumit, Tran, Grace, Mork, Maureen, Slopis, John, Kamiya, Carlos, Khatua, Soumen, Zaky, Wafik, Sadighi, Zsila
格式: Artigo
語言:Inglês
出版: Oxford University Press 2019
主題:
Pediatric Clinical Trials
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6847491/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz175.766
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