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Novel mutations in
Myoclonin1/EFHC1
in sporadic and familial juvenile myoclonic epilepsy
Neurology Medina et al. 70: 2137
Data Supplement
Four tables; four Word documents.
Files in this Data Supplement:
E1
- E-Table 1. Inclusion and exclusion criteria for JME probands; Word document.
E2
- E-Table 2. Primer sequence for Myoclonin1/EFHC1 mutation search; Word document.
E3
- E-Table 3. Polymorphisms detected in GABRA1 and CLCN2; Word document.
E4
- E-Table 4. Result of mutation analysis in 5'UTR of EFHC1 in some members of cohorts 1 and 2 compared to healthy controls; Word document.
This Article
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