Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Dystonia and CLCN1[original query] |
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| Identification of novel mutations of the CLCN1 gene for myotonia congenital in China. Neurological research 2016 Jan 38 (1): 40-4. Meng Yan-Xin, Zhao Zhe, Shen Hong-Rui, Bing Qi, Hu Ji |
| Sequence CLCN1 and SCN4A genes in patients with nondystrophic myotonia in Chinese people. Medicine 2022 7 101 (29): e29591. Meng Yan-Xin, Yu Mei, Liu Chunmiao, Zhang Haijuan, Yang Yuxiu, Zhang Ji |
- Page last reviewed:Feb 1, 2024
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