The importance of early diagnosis and treatment in treatable neuromuscular diseasesZHANG Cheng, ZHU Yu-ling557-562
The m.3243A > G mutation load in hair follicles from different scalp regions of patients with MELASLU Yuan-yuan, ZHAO Xu-tong, WANG Qing-qing, ZHANG Xiao, YUAN Yun, WANG Zhao-xia577-581
Clinical characteristics and MTMR13/SBF2 gene mutation analysis of a Charcot-Marie-Tooth disease type 4B2 Chinese familyZHU Yu-ling, LI Huan, PAN Zhi-liang, LIANG Ying-yin, LI Jing, WANG Liang, HE Ruo-jie, LIN Jin-fu, ZHANG Cheng582-588
Clinical phenotype and gene mutation of short-chain acyl-coenzyme A dehydrogenase deficiency in a Chinese familyJI Xin-na, MAO Ying-ying, GAO Zhi-jie, TAN Bo-jing, LI Yun-lin, XU Ke-ming, CHEN Qian, CHEN Shu-hua589-594
A novel mutation in GNE gene: clinical characteristics and bioinformatics analysisWANG Liang, LI Ya-qin, ZHANG Hui-li, ZHU Yu-ling, HE Ruo-jie, LI Huan, LIN Jin-fu, ZHANG Cheng595-601
Alteration of heart rate variability in patients with Parkinson's disease after subthalamic nucleus deep brain stimulation: a Meta-analysisLUO Xiao-yue, OU Ru-wei, SHANG Hui-fang602-607