APA Citatie

Mégarbané, A., Slim, R., Nürnberg, G., Ebermann, I., Nürnberg, P., & Bolz, H. J. (2009). A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness. Nature Publishing Group.

Chicago Style citaat

Mégarbané, André, Rima Slim, Gudrun Nürnberg, Inga Ebermann, Peter Nürnberg, en Hanno Jörn Bolz. A Novel VPS13B Mutation in Two Brothers With Cohen Syndrome, Cutis Verticis Gyrata and Sensorineural Deafness. Nature Publishing Group, 2009.

MLA citatie

Mégarbané, André, et al. A Novel VPS13B Mutation in Two Brothers With Cohen Syndrome, Cutis Verticis Gyrata and Sensorineural Deafness. Nature Publishing Group, 2009.