EHMT2

Publications

Carvalho LML et al. EHMT2 as a candidate gene for an autosomal recessive neurodevelopmental syndrome. Mol Neurobiol. 2025;62(5):5977-89. PMID: 39674972.

Martinez-Delgado B et al. EHMT2 loss-of-function alterations cause a Kleefstra-like syndrome. medRxiv. 2024. doi: 10.1101/2024.01.10.24300997.