Developmental and Epileptic Encephalopathy 7
Description
An autosomal dominant form of early infantile epileptic encephalopathy caused by mutation(s) in the KCNQ2 gene, encoding potassium voltage-gated channel subfamily KQT member 2.
Cell Lines
- BCHi035-A
- BCHi035-A-1
- BCHi035-A-1
- BCHi035-A-2
- BCHi035-A-3
- BCHi035-A-4
- BCHi035-A-2
- BCHi035-A-3
- BCHi035-A-4
- BCHi036-A
- BCHi036-A-1
- BCHi036-A-1
- BCHi036-A-2
- BCHi036-A-2
- BCHi036-A-3
- BCHi036-A-3
- BCHi036-A-4
- BCHi036-A-4
- BCHi037-A
- BCHi037-A-1
- BCHi037-A-1
- BCHi037-A-2
- BCHi037-A-2
- BCHi037-A-3
- BCHi037-A-3
- BCHi037-A-4
- BCHi037-A-4
- BCHi045-A
- BCHi045-A-1
- BCHi045-A-1
- BCHi045-A-2
- BCHi045-A-2
- BCHi045-A-3
- BCHi045-A-3
- BCHi045-A-4
- BCHi045-A-4
- BCHi045-A-5
- BCHi045-A-5
- BCHi046-A
- BCHi046-A-1
- BCHi046-A-1
- BCHi046-A-2
- BCHi046-A-2
- BCHi046-A-3
- BCHi046-A-3