Cite
A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human [Beta]-subunit of the Inhibitory Glycine Receptor (GLRB)
MLA
Rees, M. I., 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, vol. 67, no. 4, Oct. 2000, p. 391. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.66671062&authtype=sso&custid=ns315887.
APA
Rees, M. I., Lewis, T. M., Mortier, G., Snell, R. G., Schofield, P. R., & Owen, M. J. (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), 391.
Chicago
Rees, M.I., T.M. Lewis, G. Mortier, R.G. Snell, P.R. Schofield, and M.J. Owen. 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): 391. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsggo&AN=edsgcl.66671062&authtype=sso&custid=ns315887.