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

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/paternal-mutation-of-the-sulfonylurea-receptor-sur1-gene-and-maternal-loss-of/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Virginie Verkarre,Jean‐Christophe Fournet,Pascale de Lonlay,M S Gross-Morand,Martine Devillers,Jacques Rahier,Françis Brunelle,J.J. Robert,Claire Nihoul‐Feketé,Jean‐Marie Saudubray,Claudine Junien |
| Citations | 290 |
| DOI | 10.1172/jci4495 |
| Fields | Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.jci.org/articles/view/4495/files/pdf |
| OpenAlex ID | https://openalex.org/W2086491850 |
| PMID | 9769320 |
| Type | article |
| Year | 1998 |

## Paper authors

- [Pascale de Lonlay](https://scholariq.org/researchers/pascale-de-lonlay/)

## Paper primary topic

- [Hyperglycemia and glycemic control in critically ill and hospitalized patients](https://scholariq.org/topics/hyperglycemia-and-glycemic-control-in-critically-ill-and-hospitalized-patients/)

## Paper topics

- [Hyperglycemia and glycemic control in critically ill and hospitalized patients](https://scholariq.org/topics/hyperglycemia-and-glycemic-control-in-critically-ill-and-hospitalized-patients/)
- [Congenital Diaphragmatic Hernia Studies](https://scholariq.org/topics/congenital-diaphragmatic-hernia-studies/)
- [Neonatal Respiratory Health Research](https://scholariq.org/topics/neonatal-respiratory-health-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.