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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 10, 2023. (Total: 217827Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Charcot-Marie-Tooth Disease and MORC2[original query]
MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
Annals of neurology 2015 Dec .
Albulym Obaid M, Kennerson Marina L, Harms Matthew B, Drew Alexander P, Siddell Anna H, Auer-Grumbach Michaela, Pestronk Alan, Connolly Anne, Baloh Robert H, Zuchner Stephan, Reddel Stephen W, Nicholson Garth
MORC2 mutations in a cohort of Chinese patients with Charcot-Marie-Tooth disease type 2.
Brain : a journal of neurology 2016 Jun .
Zhao Xin, Li Xiaobo, Hu Zhengmao, Liu Lei, Xie Yongzhi, Tian Tian, Man Jianfen, Wang Juan, Zi Xiaohong, Xia Kun, Tang Beisha, Wei Xiaoming, Zhang Ru
Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China.
European journal of neurology 2021 7 28 (11): 3774-3783.
Xie Yongzhi, Lin Zhiqiang, Liu Lei, Li Xiaobo, Huang Shunxiang, Zhao Huadong, Wang Binghao, Zeng Sen, Cao Wanqian, Li Lu, Zhu Xiying, Huang Siwei, Yang Honglan, Wang Mengli, Hu Zhengmao, Wang Junling, Guo Jifeng, Shen Lu, Jiang Hong, Zuchner Stephan, Tang Beisha, Zhang Ru
Rare among Rare: Phenotypes of Uncommon CMT Genotypes.
Brain sciences 2021 12 11 (12): .
Gentile Luca, Russo Massimo, Taioli Federica, Ferrarini Moreno, Aguennouz M'Hammed, Rodolico Carmelo, Toscano Antonio, Fabrizi Gian Maria, Mazzeo An
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