Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome.Yoko Narumi-Kishimoto, Naomi Araki,Ohsuke Migita,Tomoko Kawai,Kohji Okamura,Kazuhiko Nakabayashi,Tadashi Kaname, Yuri Ozawa,Hiroshi Ozawa,Fumio Takada,Kenichiro HataEuropean Journal of Medical Genetics(2019)引用 14|浏览21暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要