Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Charcot-Marie-Tooth Disease and FGD4[original query] |
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Charcot-Marie-Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families. Annals of human genetics 2015 Sep . Hyun Young Se, Lee Jinho, Kim Hye Jin, Hong Young Bin, Koo Heasoo, Smith Alec S T, Kim Deok-Ho, Choi Byung-Ok, Chung Ki W |
Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis.
Neurology. Genetics 2019 Dec 5 (6): e375. Wei Ling, Tian Yanghua, Chen Yongping, Wei Qianqian, Chen Fangfang, Cao Bei, Wu Ying, Zhao Bi, Chen Xueping, Xie Chengjuan, Xi Chunhua, Yu Xu'en, Wang Juan, Lv Xinyi, Du Jing, Wang Yu, Shen Lu, Wang Xin, Shen Bin, Guo Qihao, Guo Li, Xia Kun, Xie Peng, Zhang Xuejun, Zuo Xianbo, Shang Huifang, Wang K |
Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease. Journal of human genetics 2019 12 65 (3): 313-323. Mortreux J, Bacquet J, Boyer A, Alazard E, Bellance R, Giguet-Valard A G, Cerino M, Krahn M, Audic F, Chabrol B, Laugel V, Desvignes J P, Béroud C, Nguyen K, Verschueren A, Lévy N, Attarian S, Delague V, Missirian C, Bonello-Palot |
Genetic variation in Charcot-Marie-Tooth genes contributes to sensitivity to paclitaxel-induced peripheral neuropathy. Pharmacogenomics 2020 7 21 (12): 841-851. Chen Yongzhen, Fang Fang, Kidwell Kelley M, Vangipuram Kiran, Marcath Lauren A, Gersch Christina L, Rae James M, Hayes Daniel F, Lavoie Smith Ellen M, Henry N Lynn, Beutler Andreas S, Hertz Daniel |
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