Myoclonus, familial, 1

MONDO:0100093

Familial cortical myoclonus caused by heterozygous mutation in the NOL3 gene on chromosome 16q22.

Also known as: myoclonus, familial cortical, FCM, MYOCL1

12 clinical trials for this condition and its sub-types, 0 tagged with Myoclonus, familial, 1 itself.

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