APA

Bröer S., Bailey C. G., Kowalczuk S., Ng C., Vanslambrouck J. M., Rodgers H., Auray-Blais C., Cavanaugh J. A., Bröer A. & Rasko J. E. J. (20081230). Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. : The Journal of clinical investigation.

Chicago

Bröer Stefan, Bailey Charles G, Kowalczuk Sonja, Ng Cynthia, Vanslambrouck Jessica M, Rodgers Helen, Auray-Blais Christiane, Cavanaugh Juleen A, Bröer Angelika and Rasko John E J. 20081230. Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. : The Journal of clinical investigation.

Harvard

Bröer S., Bailey C. G., Kowalczuk S., Ng C., Vanslambrouck J. M., Rodgers H., Auray-Blais C., Cavanaugh J. A., Bröer A. and Rasko J. E. J. (20081230). Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. : The Journal of clinical investigation.

MLA

Bröer Stefan, Bailey Charles G, Kowalczuk Sonja, Ng Cynthia, Vanslambrouck Jessica M, Rodgers Helen, Auray-Blais Christiane, Cavanaugh Juleen A, Bröer Angelika and Rasko John E J. Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. : The Journal of clinical investigation. 20081230.