Bei-sha Tang

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 422 citations

Auditory Processing, Developmental Biology, Health Sciences +13

VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

Yun Tian, Fu‐Lei Tang, Xiang-Dong Sun et al. · Molecular Brain · 2015 · 77 citations · Full text

Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism

Ji-feng Guo, Xue-wei Zhang, Li-luo Nie et al. · Journal of Neurology · 2010 · 45 citations

Neurodegenerative Diseases, Genetic Disorder, Genetics +9

Paroxysmal hypnogenic dyskinesia is associated with mutations in the <i>PRRT2</i> gene

Xiao-Rong Liu, Dan Huang, Jie Wang et al. · Neurology Genetics · 2016 · 36 citations · Full text

Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders

Chen Zhao, Jun-ling Wang, Bei-sha Tang et al. · Neurobiology of Aging · 2013 · 22 citations

Rare Diseases, Neurodegenerative Diseases, Mendelian Disorder +10