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-Reference-Cited by-同舟云学术

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

Published:1990-07 Issue:1 Volume:71 Page:164-169
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

BARBETTI FABRIZIO,RABEN NINA,KADOWAKI TAKASHI,CAMA ALESSANDRO,ACCILI DOMENICO,GABBAY KENNETH H.,MERENICH JOHN A.,TAYLOR SIMEON I.,ROTH JESSE

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/71/1/164/10508983/jcem0164.pdf

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