Myoclonic epilepsy of Lafora 2

MONDO:0800306

Any Lafora disease in which the cause of the disease is a variation in the NHLRC1 gene.

Also known as: EPM2B, Lafora disease 2, MELF2, epilepsy, progressive myoclonic, 2B, myoclonic epilepsy of Lafora 2

20 clinical trials for this condition and its sub-types, 0 tagged with Myoclonic epilepsy of Lafora 2 itself.

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