1. A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2. Issue 22 (20th November 2021) Authors: Qiu, Liang-Liang; Lin, Xiao-Dan; Xu, Guo-Rong; Wang, Li-Li; Ye, Zhi-Xian; Lin, Feng; Chen, Hai-Zhu; Lin, Min-Ting; Cai, Nai-Qing; Jin, Ming; Xu, Liu-Qing; Hu, Wei; Wang, Ning; Wang, Zhi-Qiang Editors: Guo, Li-Shao Journal: Chinese medical journal Issue: Volume 134:Issue 22(2021) Page Start: 2753 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Levodopa-Induced Ocular Dyskinesia in an Early-Onset Parkinson Disease Patient With GBA Mutation. Issue 6 (November 2021) Authors: He, Jia-Ming; Wu, Zhi-Bo; Cai, Nai-Qing; Lin, Yu Journal: Clinical neuropharmacology Issue: Volume 44:Issue 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗