1. Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. Issue 5 (May 1996) Authors: Elmslie, F V; Hutchings, S M; Spencer, V; Curtis, A; Covanis, T; Gardiner, R M; Rees, M Journal: Journal of medical genetics Issue: Volume 33:Issue 5(1996) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗