| Original language | English |
|---|---|
| Pages (from-to) | 188 |
| Number of pages | 1 |
| Journal | European Journal of Human Genetics |
| Volume | 32 |
| Issue number | Supplement 1 |
| Publication status | Published - 8 Jan 2024 |
EP09.039 KMT2C pathogenic variants result in a neurodevelopmental disorder with distinct clinical and DNA methylation features
D Rots, S Choufani, V Faundes, A Dingemans, L Vissers, T Kleefstra, S Banka, R Weksberg
Research output: Contribution to journal › Meeting Abstract › peer-review