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. Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice. Issue 1 (3rd September 2019) Authors: Li, Jin-Jing; Lin, Xiang; Tang, Cheng; Lu, Ying-Qian; Hu, Xinde; Zuo, Erwei; Li, He; Ying, Wenqin; Sun, Yidi; Lai, Lu-Lu; Chen, Hai-Zhu; Guo, Xin-Xin; Zhang, Qi-Jie; Wu, Shuang; Zhou, Changyang; Shen, Xiaowen; Wang, Qifang; Lin, Min-Ting; Ma, Li-Xiang; Wang, Ning Journal: National science review Issue: Volume 7:Issue 1(2020) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings. Issue 5 (5th March 2021) Authors: Guo, Qi-Fu; Ye, Zhi-Xian; Qiu, Liang-Liang; Lin, Xin; Lai, Jia-He; Lin, Min-Ting; Wang, Zhi-Qiang; Wang, Ning; Lin, Feng Editors: Ni, Jing Journal: Chinese medical journal Issue: Volume 134:Issue 5(2021) Page Start: 622 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Growth Hormone Deficiency in a Dopa-Responsive Dystonia Patient With a Novel Mutation of Guanosine Triphosphate Cyclohydrolase 1 Gene. (May 2015) Authors: Lin, Yu; Wang, Dan-Ni; Chen, Wan-Jin; Lin, Xiang; Lin, Min-Ting; Wang, Ning Journal: Journal of child neurology Issue: Volume 30:Number 6(2015:Jul.) Page Start: 796 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients. (4th March 2018) Authors: Wang, Dan-Ni; Wang, Zhi-Qiang; Chen, Yu-Qing; Xu, Guo-Rong; Lin, Min-Ting; Wang, Ning Journal: International journal of neuroscience Issue: Volume 128:Number 3(2018) Page Start: 199 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Short-term efficacy of repetitive transcranial magnetic stimulation in SCA3: A prospective, randomized, double-blind, sham-controlled study. (January 2023) Authors: Sikandar, Arif; Liu, Xia-Hua; Xu, Hao-Ling; Li, Ying; Lin, Yun-Qing; Chen, Xin-Yuan; Li, Gui-He; Lin, Min-Ting; Wang, Ning; Chen, Wan-Jin; Ni, Guo-Xin; Gan, Shi-Rui Journal: Parkinsonism & related disorders Issue: Volume 106(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes. (October 2019) Authors: Lin, Shan; Zeng, Jia-Bin; Zhao, Gui-Xian; Yang, Zhen-Zhen; Huang, Hui-Ping; Lin, Min-Ting; Wu, Zhi-Ying; Wang, Ning; Chen, Wan-Jin; Fang, Ling Journal: Seizure Issue: Volume 71(2019) Page Start: 322 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Variations of IGHMBP2 Gene Was Not the Major Cause of Han Chinese Patients With Non-5q-Spinal Muscular Atrophies. (August 2014) Authors: Lin, Xiang; Zhang, Qi-Jie; He, Jin; Lin, Min-Ting; Murong, Shen-Xing; Wang, Ning; Chen, Wan-Jin Other Names: Majnemer Annette guest-editor. Journal: Journal of child neurology Issue: Volume 29:Number 8(2014:Aug.) Page Start: NP35 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗