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[The phenotypes and genotypes in 314 patients with isolated methylmalonic acidemia].
Kang LL, Liu YP, Shen M, Chen ZH, Song JQ, He RX, Liu Y, Zhang Y, Dong H, Li MQ, Jin Y, Zheng H, Wang Q, Ding Y, Li XY, Li DX, Li HX, Liu XQ, Xiao HJ, Jiang YW, Xiong H, Zhang CY, Wang ZX, Yuan Y, Liang DS, Tian YP, Yang YL. Kang LL, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2020 Jun 2;58(6):468-475. doi: 10.3760/cma.j.cn112140-20200401-00339. Zhonghua Er Ke Za Zhi. 2020. PMID: 32521958 Chinese.
[Genotype and phenotype of female Dravet syndrome with PCDH19 mutations].
Liu AJ, Zhang YH, Xu XJ, Yang XL, Yang ZX, Wu Y, Liu XY, Jiang YW, Wu XR. Liu AJ, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2016 May;54(5):327-31. doi: 10.3760/cma.j.issn.0578-1310.2016.05.004. Zhonghua Er Ke Za Zhi. 2016. PMID: 27143072 Chinese.
[Phenotype study of SCN2A gene related epilepsy].
Zeng Q, Zhang YH, Yang XL, Zhang J, Liu AJ, Liu XY, Jiang YW, Wu XR. Zeng Q, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2018 Jul 2;56(7):518-523. doi: 10.3760/cma.j.issn.0578-1310.2018.07.009. Zhonghua Er Ke Za Zhi. 2018. PMID: 29996185 Chinese.
321 results