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Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
Tan D, Ge L, Fan Y, Chang X, Wang S, Wei C, Ding J, Liu A, Wang S, Li X, Gao K, Yang H, Que C, Huang Z, Li C, Zhu Y, Mao B, Jin B, Hua Y, Zhang X, Zhang B, Zhu W, Zhang C, Wang Y, Yuan Y, Jiang Y, Rutkowski A, Bönnemann CG, Wu X, Xiong H. Tan D, et al. Among authors: wang y, wang s. Orphanet J Rare Dis. 2021 Jul 19;16(1):319. doi: 10.1186/s13023-021-01950-x. Orphanet J Rare Dis. 2021. PMID: 34281576 Free PMC article.
[Clinical and laboratory screening studies on urea cycle defects].
Yang YL, Sun F, Qian N, Song JQ, Wang S, Chang XZ, Yang HY, Wang SQ, Li L, Zhang YH, Bao XH, Li M, Qi Y, Qin J, Wu XR. Yang YL, et al. Among authors: wang sq, wang s. Zhonghua Er Ke Za Zhi. 2005 May;43(5):331-4. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924745 Chinese.
[Clinical features and management of multiple sclerosis in children].
Xiong H, Zhang YH, Zhou R, Bao XH, Jiang YW, Wu Y, Wang S, Chang XZ, Fu SQ, Qin J, Wu XR. Xiong H, et al. Among authors: wang s. Zhonghua Er Ke Za Zhi. 2007 Aug;45(8):568-73. Zhonghua Er Ke Za Zhi. 2007. PMID: 18021526 Clinical Trial. Chinese.
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