KCNJ11 Mutation in One Family is Associated with Adult-Onset Rather than Neonatal-Onset Diabetes Mellitus-Reference-Cited by-同舟云学术

KCNJ11 Mutation in One Family is Associated with Adult-Onset Rather than Neonatal-Onset Diabetes Mellitus

Published:2018-09 Issue:5 Volume:4 Page:e411-e414
ISSN:2376-0605
Container-title:AACE Clinical Case Reports
language:en
Short-container-title:AACE Clinical Case Reports

Author:

Breidbart Emily,Golden Lauren,Gonzaga-Jauregui Claudia,Deng Liyong,Lanzano Patricia,LeDuc Charles,Guo JianCheng,Overton John D.,Reid Jeffery,Shuldiner Alan,Chung Wendy K.

Publisher

Elsevier BV

Reference15 articles.

1. The diagnosis and management of monogenic diabetes in children and adolescents;Hattersley;Pediatr Diabetes,2009

2. Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes;Girard;Pflugers Arch,2006

3. The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus;Yorifuji;J Clin Endocrinol Metab,2005

4. Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation;D'Amato;Diabet Med,2008

5. Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene;Bonnefond;PLoS One,2012

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. Phenotypic features, prevalence of KCNJ11‐MODY in Chinese patients with early‐onset diabetes and a literature review;Clinical Endocrinology;2024-08-27

2. MODY in China: two families carrying the KCNJ11 E229K variant;Acta Diabetologica;2023-06-10

3. Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry;Journal of Pediatric Endocrinology and Metabolism;2021-04-13