Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping.
| Autor: | Collinet, M., Berthelon, M., Bénit, P., Laborde, K., Desbuquois, B., Munnich, A., Robert, J. J., Bénit, P (AUTHOR) |
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| Zdroj: | European Journal of Pediatrics. 1998, Vol. 157 Issue 6, p456-460. 5p. |
| Databáze: | Academic Search Ultimate |
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