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pro vyhledávání: '"Kei Irie, PhD"'
Autor:
Taira Ninomaru, MD, Hideaki Okada, MD, Mika Fujishima, MD, PhD, Kei Irie, PhD, Shoji Fukushima, PhD, Akito Hata, MD
Publikováno v:
JTO Clinical and Research Reports, Vol 2, Iss 3, Pp 100145- (2021)
The spread of next-generation sequencing enables clinicians to identify rare oncogene alterations, including MET exon 14 skipping mutation, in clinical practice for NSCLC. Several tyrosine kinase inhibitors for MET exon 14 skipping mutation such as c
Externí odkaz:
https://doaj.org/article/1ecf4d948d4f4e88a0c38703ea02140e