Author:
Harvey Robert J.,Topf Maya,Harvey Kirsten,Rees Mark I.
Reference75 articles.
1. Startle syndromes;Bakker;Lancet Neurol.,2006
2. Stephenson, J.B.P. et al. (2008) Hyperekplexia: a glycinergic disorder. In Channelopathies of the Nervous System in Childhood (Zuberi, S., ed.), Clinics in Developmental Medicine, Cambridge University Press, in press.
3. Startle disease: an avoidable cause of sudden infant death;Vigevano;Lancet,1989
4. Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia;Shiang;Nat. Genet.,1993
5. Mutational analysis of familial and sporadic hyperekplexia;Shiang;Ann. Neurol.,1995
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