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About this Biochemistry, Genetics and Molecular Biology article
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. by Elmslie, F V; Hutchings, S M; Spencer, V; Curtis, A; Covanis, T; Gardiner, R M; Rees, M is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Elmslie, F V; Hutchings, S M; Spencer, V; Curtis, A; Covanis, T; Gardiner, R M; Rees, M
- Publisher
- BMJ Publishing Group; BMJ (ISSN 0022-2593)
- Published
- 1996
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)