KMT2B

Publications

Meyer E et al. Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nat Genet 2017;49(2):223e37. PMID: 27992417

Zech M, et al. Haploinsufficiency of KMT2B, encoding the lysine- specific histone methyltransferase 2B, results in early-onset generalized dystonia. Am J Hum Genet 2016;99(6):1377-1387. PMID: 27839873

Gorman KM et al. Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B. Eur J Paediatr Neurol 2018;22(2)245-256. PMID: 29289525