QuickView for KMT2D;jsessionid=55392BFD6BC030587E6DB96462C67EE5;jsessionid=4DF6118AFDDB5D060AAA8B7C41EEF16B;jsessionid=FAA8D58D833E96BD844C71DB05B27FF5 (gene)

1. Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B.
2. Child Neurology: KMT2B-Related Dystonia in a Young Child With Worsening Gait Abnormality.
3. Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset.
4. Comparison of methylation episignatures in KMT2B- and KMT2D-related human disorders.
5. Dystonic Tremor in Adult-onset DYT-KMT2B.

There were no clinical trials for KMT2D;jsessionid=55392BFD6BC030587E6DB96462C67EE5;jsessionid=4DF6118AFDDB5D060AAA8B7C41EEF16B;jsessionid=FAA8D58D833E96BD844C71DB05B27FF5