APA Citatie

Bröer, S., Bailey, C. G., Kowalczuk, S., Ng, C., Vanslambrouck, J. M., Rodgers, H., . . . Rasko, J. E. (2008). Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. American Society for Clinical Investigation.

Chicago Style citaat

Bröer, Stefan, et al. Iminoglycinuria and Hyperglycinuria Are Discrete Human Phenotypes Resulting From Complex Mutations in Proline and Glycine Transporters. American Society for Clinical Investigation, 2008.

MLA citatie

Bröer, Stefan, et al. Iminoglycinuria and Hyperglycinuria Are Discrete Human Phenotypes Resulting From Complex Mutations in Proline and Glycine Transporters. American Society for Clinical Investigation, 2008.