Exome Sequencing Identifies A Novel Homozygous Missense Atp13a2 MutationMasoom M Abbas,Shyla T Govindappa,Una-Marie Sheerin,Kailash P Bhatia,Uday B MuthaneMOVEMENT DISORDERS CLINICAL PRACTICE（2017）引用 5|浏览1暂无评分关键词Kufor-Rakeb syndrome, exome sequence, early onset atypical parkinsonismAI 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
