APA (7th ed.) Citation

Collinet, M., Berthelon, M., Bénit, P., Laborde, K., Desbuquois, B., Munnich, A., . . . Bénit, P. (1998). Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: Identification of the mutation by restriction enzyme mapping. European Journal of Pediatrics, 157(6), 456. https://doi.org/10.1007/s004310050852

Chicago Style (17th ed.) Citation

Collinet, M., M. Berthelon, P. Bénit, K. Laborde, B. Desbuquois, A. Munnich, J. J. Robert, and P. Bénit. "Familial Hyperproinsulinaemia Due to a Mutation Substituting Histidine for Arginine at Position 65 in Proinsulin: Identification of the Mutation by Restriction Enzyme Mapping." European Journal of Pediatrics 157, no. 6 (1998): 456. https://doi.org/10.1007/s004310050852.

MLA (9th ed.) Citation

Collinet, M., et al. "Familial Hyperproinsulinaemia Due to a Mutation Substituting Histidine for Arginine at Position 65 in Proinsulin: Identification of the Mutation by Restriction Enzyme Mapping." European Journal of Pediatrics, vol. 157, no. 6, 1998, p. 456, https://doi.org/10.1007/s004310050852.