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A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia
- Correspondence to: Professor A Pascotto, C Neuropsichiatria Infantile, 2° Policlinico, Via S Pansini 5, 80131, Napoli, Italy; antonio.pascotto{at}unina2.it
Citation
A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia
Publication history
- First published May 1, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics