Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplified by polymerase chain reaction.

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Published in J Clin Endocrinol Metab on July 01, 1990

Authors

F Barbetti1, N Raben, T Kadowaki, A Cama, D Accili, K H Gabbay, J A Merenich, S I Taylor, J Roth

Author Affiliations

1: Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.

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