Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping.

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Bibliographic Details
Title: Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping.
Authors: Collinet, M., Berthelon, M., Bénit, P., Laborde, K., Desbuquois, B., Munnich, A., Robert, J. J., Bénit, P (AUTHOR)
Source: European Journal of Pediatrics. 1998, Vol. 157 Issue 6, p456-460. 5p.
Database: Academic Search Ultimate
Description
ISSN:03406199
DOI:10.1007/s004310050852