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3. [KMT2B variants responsible for children dystonia 28: report of two cases]. Dai LF, Ding CH, Fang T, Xie ZH, Liu TH, Zhang WH, Wang XH, Ren XT, Liu M, Tian XJ, Wu HS, Fang F. Zhonghua Er Ke Za Zhi; 2019 Jul 02; 57(7):564-566. PubMed ID: 31269560 [Abstract] [Full Text] [Related]
4. Update on KMT2B-Related Dystonia. Zech M, Lam DD, Winkelmann J. Curr Neurol Neurosci Rep; 2019 Nov 25; 19(11):92. PubMed ID: 31768667 [Abstract] [Full Text] [Related]
13. Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B. Gorman KM, Meyer E, Kurian MA. Eur J Paediatr Neurol; 2018 Mar 01; 22(2):245-256. PubMed ID: 29289525 [Abstract] [Full Text] [Related]
15. Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset. Mirza-Schreiber N, Zech M, Wilson R, Brunet T, Wagner M, Jech R, Boesch S, Škorvánek M, Necpál J, Weise D, Weber S, Mollenhauer B, Trenkwalder C, Maier EM, Borggraefe I, Vill K, Hackenberg A, Pilshofer V, Kotzaeridou U, Schwaibold EMC, Hoefele J, Waldenberger M, Gieger C, Peters A, Meitinger T, Schormair B, Winkelmann J, Oexle K. Brain; 2022 Apr 18; 145(2):644-654. PubMed ID: 34590685 [Abstract] [Full Text] [Related]