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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and MPZ[original query]
Next-generation sequencing-based molecular diagnosis of neonatal hypotonia in Chinese Population.
Scientific reports 2016 6 29088.
Wang Yan, Peng Wei, Guo Hong-Yan, Li Hui, Tian Jie, Shi Yu-Jing, Yang Xiao, Yang Yao, Zhang Wan-Qiao, Liu Xin, Liu Guan-Nan, Deng Tao, Sun Yi-Min, Xing Wan-Li, Cheng Jing, Feng Zhi-Ch
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?
Brain and behavior 2016 Mar e00451.
Werheid Friederike, Azzedine Hamid, Zwerenz Eva, Bozkurt Ahmet, Moeller Marcus J, Lin Lilian, Mull Michael, Häusler Martin, Schulz Jörg B, Weis Joachim, Claeys Kristl
Genotype-phenotype characteristics and baseline natural history of Chinese myelin protein zero gene related neuropathy patients.
European journal of neurology 2023 1 30 (4): 1069-1079.
Lei Liu, Xiaobo Li, Zhiqiang Lin, Yongzhi Xie, Shunxiang Huang, Huadong Zhao, Beisha Tang, Ruxu Zha
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