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Successful treatment of a lung adenocarcinoma patient with a novel EGFR exon 20-ins mutation with afatinib: A case report
RATIONALE: Comprehensive genomic profiling for non-small cell lung cancer (NSCLC) is likely to identify more patients with rare genetic alterations, including uncommon epidermal growth factor receptor (EGFR) gene mutation. PATIENT CONCERNS: A 63-year-old Chinese woman who had never smoked visited ou...
Guardat en:
| Publicat a: | Medicine (Baltimore) |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Health
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6344163/ https://ncbi.nlm.nih.gov/pubmed/30608413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000013890 |
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