Simpson, M., Cross, H., Proukakis, C., Priestman, D., Neville, D., Reinkensmeier, G., . . . Crosby, A. (2004). Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.
Chicago Style (17th ed.) CitationSimpson, M., et al. Infantile-onset Symptomatic Epilepsy Syndrome Caused by a Homozygous Loss-of-function Mutation of GM3 Synthase. 2004.
MLA (9th ed.) CitationSimpson, M., et al. Infantile-onset Symptomatic Epilepsy Syndrome Caused by a Homozygous Loss-of-function Mutation of GM3 Synthase. 2004.
Warning: These citations may not always be 100% accurate.