✦ LIBER ✦
The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions
✍ Scribed by Ortrud K. Steinlein; M. Villain; C. Korenke
- Book ID
- 119366855
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 198 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1059-1311
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