Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations

Mutations in the high-affinity sulfonylurea receptor (SUR)-1 cause one of the severe recessively inherited diffuse forms of congenital hyperinsulinism or, when associated with loss of heterozygosity, focal adenomatosis. We hypothesized that SUR1 mutations would render the β-cell insensitive to sulfo...

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Autors principals: Grimberg, A., Ferry, R.J., Kelly, A., Koo-McCoy, S., Polonsky, K., Glaser, B., Permutt, M.A., Aguilar-Bryan, L., Stafford, D., Thornton, P.S., Baker, L., Stanley, Charles A.
Format: Artigo
Idioma:Inglês
Publicat: 2001
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3313678/
https://ncbi.nlm.nih.gov/pubmed/11272143
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