Identification of a novel de novo KMT2B variant in a Greek dystonia patient via exome sequencing genotype–phenotype correlations of all published cases

MLA

Georgia Xiromerisiou, et al. “Identification of a Novel de Novo KMT2B Variant in a Greek Dystonia Patient via Exome Sequencing Genotype–phenotype Correlations of All Published Cases.” Molecular Biology Reports, vol. 48, Dec. 2020, pp. 371–79. EBSCOhost, https://doi.org/10.1007/s11033-020-06057-3.

APA

Georgia Xiromerisiou, Dimitrios Rikos, Panagiotis Ntellas, Katerina Dadouli, Georgios M. Hadjigeorgiou, Chrysoula Marogianni, Cleanthi Spanaki, & Despoina Georgouli. (2020). Identification of a novel de novo KMT2B variant in a Greek dystonia patient via exome sequencing genotype–phenotype correlations of all published cases. Molecular Biology Reports, 48, 371–379. https://doi.org/10.1007/s11033-020-06057-3

Chicago

Georgia Xiromerisiou, Dimitrios Rikos, Panagiotis Ntellas, Katerina Dadouli, Georgios M. Hadjigeorgiou, Chrysoula Marogianni, Cleanthi Spanaki, and Despoina Georgouli. 2020. “Identification of a Novel de Novo KMT2B Variant in a Greek Dystonia Patient via Exome Sequencing Genotype–phenotype Correlations of All Published Cases.” Molecular Biology Reports 48 (December): 371–79. doi:10.1007/s11033-020-06057-3.