The single nucleotide variant at c.662A>G in human RRM2B is a loss-of-function mutation

Yen Tzu Tseng, Shang Wei Li, Wei Chun HuangFu, Yun Yen, I. Hsuan Liu

研究成果: 雜誌貢獻 › 文章 › 同行評審

指紋

深入研究「The single nucleotide variant at c.662A>G in human RRM2B is a loss-of-function mutation」主題。共同形成了獨特的指紋。

Medicine & Life Sciences