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myoclonus epilepsy of Unverricht-Lundborg (EPM1)
associated with mutations in gene for cystatin B.
Interactions
disease interactions
General
genetic disease of the central nervous system
myoclonic epilepsy
Database Correlations
OMIM 254800
References
- Lafreniere et al. Nature Genetics 15:298-302 1997
- Virtaneva et al. Nature Genetics 15:393-6 1997
- Epilepsy Foundation: Unverricht-Lundborg Disease
https://www.epilepsy.com/learn/professionals/about-epilepsy-seizures/overview-epilepsy-syndromes/unverricht-lundborg-disease