A novel optineurin truncation mutation identified in a consanguineous Palestinian family with Amyotrophic Lateral Sclerosis confirms loss of function as a disease mechanismMarc Gotkine,Martina de Majo,Wong Chun Hao,Simon Topp,Moein Kanaan, Rachel Michaelson-Cohen,Silvina Epsztejn Litman, Rachel Eigess,Agnes L. Nishimura,Bradley Smith,Christopher ShawF1000Research（2016）引用 1|浏览12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
