Xuerong Leng

Gain-of-function mutation p.Arg225Cys in SCN11A causes familial episodic pain and contributes to essential tremor

Xuerong Leng, Xiaohong Qi, Yongtao Zhou et al. · Journal of Human Genetics · 2017 · 40 citations

Essential Tremor, Molecular Neuroscience, Mendelian Disorder +8

Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease

Ye Wu, Yanxia Pan, Li Du et al. · Journal of Human Genetics · 2009 · 26 citations · Full text

Engineering, Autoimmune Disease, Disease Mechanism +14

Fifteen Novel EIF2B1-5 Mutations Identified in Chinese Children with Leukoencephalopathy with Vanishing White Matter and a Long Term Follow-Up

Haihua Zhang, Lifang Dai, Na Chen et al. · PLoS ONE · 2015 · 20 citations · Full text

Founder Mutation, Chinese Children, Genetic Disorder +15

Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter disease

Xuerong Leng, Ye Wu, Xuemin Wang et al. · Journal of Human Genetics · 2011 · 19 citations · Full text

Engineering, Disease Mechanism, Clinical Translation +12

Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagy

Na Chen, Lifang Dai, Yuwu Jiang et al. · Brain and Development · 2015 · 13 citations

Cell Autophagy, Mitophagy, Signal Transduction +9