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Did you mean deharo yang[Author] (2 results)?
Loss of function of CMPK2 causes mitochondria deficiency and brain calcification.
Zhao M, Su HZ, Zeng YH, Sun Y, Guo XX, Li YL, Wang C, Zhao ZY, Huang XJ, Lin KJ, Ye ZL, Lin BW, Hong S, Zheng J, Liu YB, Yao XP, Yang D, Lu YQ, Chen HZ, Zuo E, Yang G, Wang HT, Huang CW, Lin XH, Cen Z, Lai LL, Zhang YK, Li X, Lai T, Lin J, Zuo DD, Lin MT, Liou CW, Kong QX, Yan CZ, Xiong ZQ, Wang N, Luo W, Zhao CP, Cheng X, Chen WJ. Zhao M, et al. Among authors: yang d. Cell Discov. 2022 Nov 29;8(1):128. doi: 10.1038/s41421-022-00475-2. Cell Discov. 2022. PMID: 36443312 Free PMC article.
LRP10 in autosomal-dominant Parkinson's disease.
Chen Y, Cen Z, Zheng X, Pan Q, Chen X, Zhu L, Chen S, Wu H, Xie F, Wang H, Yang D, Wang L, Zhang B, Luo W. Chen Y, et al. Among authors: yang d. Mov Disord. 2019 Jun;34(6):912-916. doi: 10.1002/mds.27693. Epub 2019 Apr 9. Mov Disord. 2019. PMID: 30964957
Genetic profile of Chinese patients with Charcot-Marie-Tooth disease.
Ouyang ZY, Chen Y, Qin DQ, Cen ZD, Zheng XS, Xie F, Chen S, Wang HT, Yang DH, Chen XH, Wang LB, Zhang BR, Luo W. Ouyang ZY, et al. Chin Med J (Engl). 2020 Nov 5;133(21):2633-2634. doi: 10.1097/CM9.0000000000001095. Chin Med J (Engl). 2020. PMID: 32941234 Free PMC article. No abstract available.
MYORG Mutation Heterozygosity Is Associated With Brain Calcification.
Chen Y, Cen Z, Chen X, Wang H, Chen S, Yang D, Fu F, Wang L, Liu P, Wu H, Zheng X, Xie F, Ouyang Z, Zhang Y, Zhou Y, Huang X, Wang F, Huang G, An H, Liang Y, Hong W, Wang A, Huang S, Chen W, Yin L, Yang Y, Huang H, Zeng R, Zhao N, Jiang B, Zhang B, Luo W; Chinese PFBC Study Group. Chen Y, et al. Among authors: yang d. Mov Disord. 2020 Apr;35(4):679-686. doi: 10.1002/mds.27973. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951047
45 results