A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy (Q81892359)
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scientific article published on 03 August 2008
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy |
scientific article published on 03 August 2008 |
Statements
A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy (English)
Iori Ohmori
Mamoru Ouchida
Takafumi Miki
Nobuyoshi Mimaki
Shigeki Kiyonaka
Teiichi Nishiki
Kazuhito Tomizawa
Yasuo Mori
Hideki Matsui
3 August 2008