Work

Analysis of clinical and genomic features in a Chinese cohort with NRG1 variations: a retrospective study

Year: 2026
Type: article
Study design: Observational Study
Abstract: Background: fusions and single nucleotide variants (SNVs) in a Chinese NSCLC cohort. Methods: alterations and their correlations with clinical characteristics, co-mutation landscapes, and treatment outcomes. Results: -positive patients. Conclusions: fusions and SNVs in NSCLC. These findings emphasize the important role of molecular profiling for precision diagnosis and individualized treatment of NSCLC.
Language: English
Field: Medicine
Open Access status: diamond
OpenAlex ID: W7128717901
FWCI:
Cites:
Cited by:
Related to: