Thought of distinguishing pathogenic gene mutation from no harm mutation in clinical practiceZHANG Cheng557-560
Progress in research on molecular mechanism of facioscapulohumeral muscular dystrophyLIN Xiao-dan, HE Jun-jie, CHEN Wan-jin, WANG Ning, WANG Zhi-qiang573-577
Advances in mechanism research of pain in Parkinson's diseaseLIU Hui, OU Ru-wei, SHANG Hui-fang586-589
Social and psychological survey on paroxysmal kinesigenic dyskinesia patients in ChinaTIAN Wo-tu, HUANG Xiao-jun, LIANG Gui-ling, ZHU Chen-xi, SHEN Ying, FANG Yu, CHEN Mu-han, SHEN Jun-yi, CHEN Sheng-di, CAO Li590-596
Clinical and genetic analysis of juvenile-onset Huntington's disease: 10 cases reportHAO Ying, CHEN Yuan-yuan, ZHANG Jin, MA Hui-zi, GU Wei-hong597-602
Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth diseaseHE Jin, XU Guo-rong, LIN Han, WANG Ning, CHEN Wan-jin603-608
Limb-girdle muscular dystrophy type 2D: clinical and genetic analysis of a familyOU Li-yu, SUN Yi-ming, LI Jing, WANG Liang, LI Huan, ZENG Ying, LIANG Ying-yin, ZHANG Cheng609-615
