- KMT2B Rare Missense Variants in Generalized Dystonia2017 | 1. lékařská fakulta
- KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes2018 | 1. lékařská fakulta
- Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset2022 | 1. lékařská fakulta
- Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing2017 | 1. lékařská fakulta