Familial hyperproinsulinemia: partial characterization of circulating proinsulin-like material.

Familial hyperproinsulinemia is an autosomal dominant defect that is associated with strikingly elevated levels of serum proinsulin-like material. Our studies show that trypsin converts familial hyperproinsulinemia proinsulin to insulin more slowly than it converts a 131I-labeled porcine proinsulin...

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Detalles Bibliográficos
Main Authors: Gabbay, K H, Bergenstal, R M, Wolff, J, Mako, M E, Rubenstein, A H
Formato: Artigo
Idioma:Inglês
Publicado: 1979
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC383713/
https://ncbi.nlm.nih.gov/pubmed/288074
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