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

1. Child Neurology: KMT2B-Related Dystonia in a Young Child With Worsening Gait Abnormality.
2. Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset.
3. Comparison of methylation episignatures in KMT2B- and KMT2D-related human disorders.
4. Dystonic Tremor in Adult-onset DYT-KMT2B.
5. A New Pathologic KMT2B Variant Associated with Childhood Onset Dystonia Presenting as Variable Pheno…

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