Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth disease by Jin HE, Guo-rong XU, Han LIN, Ning WANG, Wan-jin CHEN

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Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis by Liu-Qing Xu, Wei Hu, Qi-Fu Guo, Lu-Lu Lai, Guo-Rong Xu, Wan-Jin Chen, Wan-Jin Chen, Ning Wang, Ning Wang, Qi-Jie Zhang, Qi-Jie Zhang

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A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy by Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu

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Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency by Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui

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A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2 by Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo

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