✦ LIBER ✦
A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy
✍ Scribed by Iori Ohmori; Mamoru Ouchida; Takafumi Miki; Nobuyoshi Mimaki; Shigeki Kiyonaka; Teiichi Nishiki; Kazuhito Tomizawa; Yasuo Mori; Hideki Matsui
- Book ID
- 113812244
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 498 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0969-9961
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