Associated Papers
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature.
Yoganathan S et al.
Epilepsia, 2024
Assessment of Interlaboratory Variation in the Interpretation of Genomic Test Results in Patients With Epilepsy.
SoRelle JA et al.
Jama Network Open, 2020
32347949 (PubMed )
Supplement: jamanetwopen-3-e203812-s001.pdf
A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
Zastrow DB et al.
Journal of Genetic Counseling, 2019
Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy.
Burke EA et al.
Journal of Neurogenetics, 0
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