Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia

Rea, Ruth, Tijssen, Marina A, Herd, Colin, Frants, Rune R and Kullmann, Dimitri M (2002) Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia. European Journal Of Neuroscience, 16 (2). pp. 186-196. ISSN 0953-816X

Full text not available from this repository.
Item Type: Article
Additional Information: UCL Institute of Neurology, London, UK
Schools and Departments: School of Life Sciences > Neuroscience
Subjects: Q Science > QP Physiology > QP0351 Neurophysiology and neuropsychology > QP0361 Nervous system
Depositing User: Ruth Staras
Date Deposited: 14 Jun 2013 13:58
Last Modified: 14 Jun 2013 13:58
URI: http://sro.sussex.ac.uk/id/eprint/45391
📧 Request an update