Congenital hyperinsulinism in two siblings with ABCC8 mutation: same genotype, different phenotypes-Reference-Cited by-同舟云学术

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Congenital hyperinsulinism in two siblings with ABCC8 mutation: same genotype, different phenotypes

Published:2018-10 Issue:5 Volume:62 Page:560-565
ISSN:2359-3997
Container-title:Archives of Endocrinology and Metabolism
language:en
Short-container-title:

Author:

Sousa-Santos Francisco,Simões Helder,Castro-Feijóo Lidia,Rodríguez Paloma Cabanas,Fernández-Marmiesse Ana,Fiaño Rebeca Saborido,Rego Teresa,Carracedo Ángel,Conde Jesús Barreiro

Publisher

Archives of Endocrinology and Metabolism

Subject

Endocrinology, Diabetes and Metabolism

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability;International Journal of Molecular Sciences;2024-05-19

2. Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants with Congenital Hyperinsulinism;Case Reports in Endocrinology;2021-05-13

3. Epileptic phenotype in late-onset hyperinsulinemic hypoglycemia successfully treated by diazoxide;Journal of Pediatric Endocrinology and Metabolism;2021-03-04

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