✦ LIBER ✦
Vohwinkel Syndrome secondary to missense mutation D66H in GJB2 gene (connexin 26) can include epileptic manifestations
✍ Scribed by Pedro J. Serrano Castro; Cristina Naranjo Fernandez; Pablo Quiroga Subirana; Manuel Payan Ortiz
- Book ID
- 116880636
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 186 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1059-1311
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