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1.
Krenn, M.* et al.: ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsy. Seizure 131, 454-457 (2025)
2.
Krenn, M.* et al.: Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1B. Seizure 87, 25-29 (2021)