article · Technology in Cancer Research & Treatment
The abstract on record is too brief for a reliable plain-language summary, so none has been generated.
Our results regarding the proportion of samples with actionable mutations demonstrate the value of NGS testing for NSCLC patients in a real-world clinical diagnostic setting.
This page summarises published work. The authoritative version sits with the publisher.
DOI: 10.1177/15330338241288907
Is something wrong with this record? Report it or request removal.
Discussion
Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.
No discussion yet. Open the first thread.
New to MARATTO™? Create a free account.
