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October 1, 1998Journal of Clinical InvestigationOpen Access

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

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Authors

VVVirginie VerkarreInsermJFJean‐Christophe FournetCentre de Neurophysique Physiologie et PathologiePLPascale de LonlayDélégation Paris 5

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Cite This Study

Verkarre et al. (1998) studied this question.

synapsesocial.com/papers/6a82434bf10a9fcdd646c628https://doi.org/10.1172/jci4495
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy1996 · 444 citations
  2. 2Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews1996 · 247 citations
  3. 3Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation1998 · 571 citations
  4. 4Mutations in the Sulfonylurea Receptor Gene in Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy1995 · 818 citations