SLC1A7 mutation is a cause of the autosomal dominant form of Parkinson's diseaseA. Kishore,M. Marc Sturm, F. Raimondi,P. Lichtner,A. Sreelatha,N. Casadei,C. Blauwendraat,G. Sarma,R. Kruger,A. Zimprich,A. Singleton,T. Gasser,O. Riess, M. SharmaMOVEMENT DISORDERS（2023）引用 0|浏览10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
