Vohwinkel Syndrome secondary to missense mutation D66H in...

Seizure 2010 Vol. 19; Iss. 2

Vohwinkel Syndrome secondary to missense mutation D66H in GJB2 gene (connexin 26) can include epileptic manifestations

Pedro J. Serrano Castro, Cristina Naranjo Fernandez, Pablo Quiroga Subirana, Manuel Payan Ortiz
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Volume:
19
Year:
2010
Language:
english
DOI:
10.1016/j.seizure.2009.11.009
File:
PDF, 186 KB
english, 2010
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