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Myotonia congenita: novel mutations in CLCN1 gene.
Liu XL, Huang XJ, Shen JY, Zhou HY, Luan XH, Wang T, Chen SD, Wang Y, Tang HD, Cao L. Liu XL, et al. Among authors: cao l. Channels (Austin). 2015;9(5):292-8. doi: 10.1080/19336950.2015.1075676. Epub 2015 Aug 11. Channels (Austin). 2015. PMID: 26260254 Free PMC article.
Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.
Huang XJ, Wang T, Wang JL, Liu XL, Che XQ, Li J, Mao X, Zhang M, Bi GH, Wu L, Zhang Y, Wang JY, Shen JY, Tang BS, Cao L, Chen SD. Huang XJ, et al. Among authors: cao l. Neurology. 2015 Nov 3;85(18):1546-53. doi: 10.1212/WNL.0000000000002079. Epub 2015 Oct 7. Neurology. 2015. PMID: 26446061
Novel ATM mutations with ataxia-telangiectasia.
Liu XL, Wang T, Huang XJ, Zhou HY, Luan XH, Shen JY, Chen SD, Cao L. Liu XL, et al. Among authors: cao l. Neurosci Lett. 2016 Jan 12;611:112-5. doi: 10.1016/j.neulet.2015.11.036. Epub 2015 Nov 25. Neurosci Lett. 2016. PMID: 26628246
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