Progressive myoclonic epilepsy type 6

MONDO:0013526

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the GOSR2 gene.

Also known as: EPM6, GOSR2 progressive myoclonic epilepsy, GOSR2-related progressive myoclonus ataxia, North Sea progressive myoclonus epilepsy, PME type 6, epilepsy, progressive myoclonic 6, epilepsy, progressive myoclonic, type 6, progressive myoclonic epilepsy caused by mutation in GOSR2

7 clinical trials for this condition and its sub-types, 0 tagged with Progressive myoclonic epilepsy type 6 itself.

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↑ Progressive myoclonus epilepsy (12)

Including sub-types (7) Tagged with Progressive myoclonic epilepsy type 6 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.