Reply to: “THAP11 CAG Expansion Beyond Chinese‐Ancestry Cohorts: An Examination of 1000 Genomes and UK Biobank” von Wei, Cuijie, Chen, Zhao, Tan, Dandan, Jiang, Hong, Zhong, Nanbert, Xiong, Hui

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CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia von Tan, Dandan, Wei, Cuijie, Chen, Zhao, Huang, Yu, Deng, Jianwen, Li, Jingjing, Liu, Yidan, Bao, Xinhua, Xu, Jin, Hu, Zhengmao, Wang, Suxia, Fan, Yanbin, Jiang, Yizheng, Wu, Ye, Wu, Yuan, Wang, Shuang, Liu, Panyan, Zhang, Yuehua, Yang, Zhixian, Jiang, Yuwu, Zhang, Hong, Hong, Daojun, Zhong, Nanbert, Jiang, Hong, Xiong, Hui

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Multifunctional Transcription Factor YABBY6 Regulates Morphogenesis, Drought and Cold Stress Responses in Rice von Zuo, Jia, Wei, Cuijie, Liu, Xiaozhu, Jiang, Libo, Gao, Jing

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Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy von Zhang, Shu, Qin, Dongdong, Wu, Liwen, Li, Man, Song, Lifang, Wei, Cuijie, Lu, Chunling, Zhang, Xiaoli, Hong, Siqi, Ma, Mingming, Wu, Shiwen

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Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis von Wei, Cuijie, Liang, Zhenwei, Wu, Ying, Liu, Shan, Qiu, Jianxing, Meng, Lingchao, Li, Chunde, Li, Shuang, Bao, Xinhua, Wang, Zhaoxia, Chen, Luzeng, Xiong, Hui

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Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre von Zhang, Yu, Yan, Hui, Liu, Jieyu, Yan, Huifang, Ma, Yinan, Wei, Cuijie, Wang, Zhaoxia, Xiong, Hui, Chang, Xingzhi

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Treatment of childhood intraneural perineurioma: A case report and literature review von Li, Rongpei, Zhang, Yao, Li, Guanggui, Wei, Cuijie, Xiong, Hui, Chang, Xingzhi

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Correlation of Phenotype-Genotype and Protein Structure in RYR1 -Related Myopathy von Chang, Xingzhi, Wei, Risheng, Wei, Cuijie, Liu, Jieyu, Qin, Lun, Yan, Hui, Ma, Yinan, Wang, Zhaoxia, Xiong, Hui

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Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers von Zhang, Jianzhao, Ji, Taoyun, Chen, Qian, Jiang, Yanan, Cheng, Huan, Zheng, Ping, Ma, Wenqiang, Lei, Ting, Zhang, Yao, Jin, Yiwen, Wei, Cuijie, Wu, Ye, Chang, Xingzhi, Bao, Xinhua, Zhang, Yuehua, Xiong, Hui, Ji, Xinna, Feng, Shuo, Ren, Haitao, Yang, Jian, Jiang, Yuwu

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Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort von Tan, Dandan, Ge, Lin, Fan, Yanbin, Chang, Xingzhi, Wang, Shuang, Wei, Cuijie, Ding, Juan, Liu, Aijie, Wang, Shuo, Li, Xueying, Gao, Kai, Yang, Haipo, Que, Chengli, Huang, Zhen, Li, Chunde, Zhu, Ying, Mao, Bing, Jin, Bo, Hua, Ying, Zhang, Xiaoli, Zhang, Bingbing, Zhu, Wenhua, Zhang, Cheng, Wang, Yanjuan, Yuan, Yun, Jiang, Yuwu, Rutkowski, Anne, Boennemann, Carsten G., Wu, Xiru, Xiong, Hui

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Congenital muscular dystrophies in China von Ge, Lin, Zhang, Cheng, Wang, Zhaoxia, Chan, Sophelia H.S., Zhu, Wenhua, Han, Chunxi, Zhang, Xiaoli, Zheng, Hong, Wu, Liwen, Jin, Bo, Shan, Jingli, Mao, Bing, Zhong, Jianmin, Peng, Xiaoyin, Cheng, Yaying, Hu, Jun, Sun, Yan, Lu, Junlan, Hua, Ying, Zhu, Sainan, Wei, Cuijie, Wang, Shuo, Jiao, Hui, Yang, Haipo, Fu, Xiaona, Fan, Yanbin, Chang, Xingzhi, Wang, Shuang, Bao, Xinhua, Zhang, Yuehua, Wang, Jingmin, Wu, Ye, Jiang, Yuwu, Yuan, Yun, Rutkowski, Anne, Bönnemann, Carsten G., Wei, Wei, Wu, Xiru, Xiong, Hui

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Scoliosis Orthopedic Surgery Combined With Nusinersen Intrathecal Injection Significantly Improved the Outcome of Spinal Muscular Atrophy Patient: A Case Report von Xu, Beiyu, Wei, Cuijie, Hu, Xiao, Li, Wenzhu, Huang, Zhen, Que, Chengli, Qiu, Jianxing, Li, Chunde, Xiong, Hui

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A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients von Song, Danyu, Fu, Xiaona, Ge, Lin, Chang, Xingzhi, Wei, Cuijie, Liu, Jieyu, Yang, Haipo, Qu, Suqing, Bao, Xinhua, Toda, Tatsushi, Wu, Xiru, Xiong, Hui

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Unique genotype-phenotype correlations within LAMA2 -related limb girdle muscular dystrophy in Chinese patients von Huang, Xiuli, Tan, Dandan, Zhang, Zaiqiang, Ge, Lin, Liu, Jieyu, Ding, Juan, Yang, Haipo, Wei, Cuijie, Chang, Xingzhi, Yuan, Yun, Yan, Chuanzhu, Xiong, Hui

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Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients von Fan, Yanbin, Xu, Zhifei, Li, Xing, Gao, Feng, Guo, Enyu, Chang, Xingzhi, Wei, Cuijie, Zhang, Cheng, Yu, Qing, Que, Chengli, Xiao, Jiangxi, Yan, Chuanzhu, Wang, Zhaoxia, Yuan, Yun, Xiong, Hui

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FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies von Fu, Xiaona, Yang, Haipo, Wei, Cuijie, Jiao, Hui, Wang, Shuo, Yang, Yanling, Han, Chunxi, Wu, Xiru, Xiong, Hui

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Juvenile Generalized Myasthenia Gravis With AChR and MuSK Antibody Double Positivity: A Case Report With a Review of the Literature von Ge, XiuShan, Wei, CuiJie, Dong, Hui, Zhang, YueHua, Bao, XinHua, Wu, Ye, Song, DanYu, Hao, HongJun, Xiong, Hui

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HPLC-PDA combined with chemometrics for chemical markers of Paeoniae Radix Alba before and after sulfur-fumigated von Jia, Xiaozhou, Liang, Yueyi, Chen, Fang, Liu, Xiaoxia, Wei, Cuijie, Ding, Qing, Chen, Xiangdong, Sun, Dongmei, Wei, Mei

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RNA sequencing facilitates the identification of genetic causes of Duchenne muscular dystrophy and proposes a stepwise DMD diagnostic procedure von Luo, Huaxia, Liu, Yidan, Wei, Cuijie, Xiong, Hui

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Risdiplam in Type 1 Spinal Muscular Atrophy von Baranello, Giovanni, Darras, Basil T, Day, John W, Deconinck, Nicolas, Klein, Andrea, Masson, Riccardo, Mercuri, Eugenio, Rose, Kristy, El-Khairi, Muna, Gerber, Marianne, Gorni, Ksenija, Khwaja, Omar, Kletzl, Heidemarie, Scalco, Renata S, Seabrook, Timothy, Fontoura, Paulo, Servais, Laurent

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