Manganese Transport Disorder: Novel Slc30a10 Mutations And Early PhenotypesMarialuisa Quadri,Mahesh Kamate,Suvasini Sharma,Simone Olgiati,Josja Graafland,Guido J Breedveld,Indu Kori,Virupaxi Hattiholi,Puneet Jain,Satinder Aneja,Atin Kumar,Parveen Gulati,Medha Goel,Bibek Talukdar,Vincenzo BonifatiMOVEMENT DISORDERS（2015）引用 45|浏览39暂无评分关键词dystonia, genetics, manganese, SLC30A10, metabolic inherited diseaseAI 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
