Rees, M., Lewis, T., Mortier, G., Snell, R., Schofield, P., & Owen, M. (2000). A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). American Journal of Human Genetics, 67(4), pp. 391-393.

Rees, Mark, Trevor Lewis, Geert Mortier, Russell Snell, Peter Schofield, and Mike Owen. "A Transient Hyperekplexia Phenotype Associated With Compound Heterozygote Mutations in the Human Beta-subunit of the Inhibitory Glycine Receptor (GLRB)." American Journal of Human Genetics 67, no. 4 (2000): 391-393.

Rees, Mark, et al. "A Transient Hyperekplexia Phenotype Associated With Compound Heterozygote Mutations in the Human Beta-subunit of the Inhibitory Glycine Receptor (GLRB)." American Journal of Human Genetics 67.4 (2000): 391-393.