Rees, M., Andrew, M., Jawad, S., & Owen, M. J. (1994). Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Human Molecular Genetics, 3(12), pp. 2175-2179.

Rees, Mark, Mark Andrew, Saeed Jawad, and Mike J. Owen. "Evidence for Recessive As Well As Dominant Forms of Startle Disease (hyperekplexia) Caused By Mutations in the Alpha 1 Subunit of the Inhibitory Glycine Receptor." Human Molecular Genetics 3, no. 12 (1994): 2175-2179.

Rees, Mark, Mark Andrew, Saeed Jawad, and Mike J. Owen. "Evidence for Recessive As Well As Dominant Forms of Startle Disease (hyperekplexia) Caused By Mutations in the Alpha 1 Subunit of the Inhibitory Glycine Receptor." Human Molecular Genetics 3.12 (1994): 2175-2179.