APA (7e ed.) Bronvermelding

Beer, N., Osbak, K., van de Bunt, M., Tribble, N., Steele, A., Wensley, K., . . . Gloyn, A. (2012). Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.

Chicago (17e ed.) Bronvermelding

Beer, N., et al. Insights into the Pathogenicity of Rare Missense GCK Variants from the Identification and Functional Characterization of Compound Heterozygous and Double Mutations Inherited in Cis. 2012.

MLA (9e ed.) Bronvermelding

Beer, N., et al. Insights into the Pathogenicity of Rare Missense GCK Variants from the Identification and Functional Characterization of Compound Heterozygous and Double Mutations Inherited in Cis. 2012.