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Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22.
Li M, Liu F, Hao X, Fan Y, Li J, Hu Z, Shi J, Fan L, Zhang S, Ma D, Guo M, Xu Y, Shi C. Li M, et al. Among authors: ma d. Front Mol Neurosci. 2022 Jun 23;15:919199. doi: 10.3389/fnmol.2022.919199. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35813061 Free PMC article.
GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders.
Fan Y, Shen S, Yang J, Yao D, Li M, Mao C, Wang Y, Hao X, Ma D, Li J, Shi J, Guo M, Li S, Yuan Y, Liu F, Yang Z, Zhang S, Hu Z, Fan L, Liu H, Zhang C, Wang Y, Wang Q, Zheng H, He Y, Song B, Xu Y, Shi C. Fan Y, et al. Among authors: ma d. Ann Neurol. 2022 May;91(5):704-715. doi: 10.1002/ana.26325. Epub 2022 Mar 8. Ann Neurol. 2022. PMID: 35152460
9,710 results