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Letter |
Novel somatic and germline mutations in intracranial germ cell tumours
Intracranial germ cell tumours are rare tumours affecting mainly male adolescents, mainly in Asia; here the authors identify frequent mutations in the KIT/RAS and AKT/mTOR signalling pathways as well as rare germline variants in JMJD1C, suggesting potential therapeutic strategies focusing on the inhibition of KIT/RAS activation and the AKT1/mTOR pathway.
- Linghua Wang
- , Shigeru Yamaguchi
- & Ching C. Lau