Detection of KCNJ11 Gene Mutations in a Family with Neonatal Diabetes Mellitus-Reference-Cited by-同舟云学术

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Detection of KCNJ11 Gene Mutations in a Family with Neonatal Diabetes Mellitus

Published:2012-04 Issue:2 Volume:16 Page:109-114
ISSN:1177-1062
Container-title:Molecular Diagnosis & Therapy
language:en
Short-container-title:Mol Diagn Ther

Author:

Abbasi Farzaneh,Saba Sadaf,Ebrahim-Habibi Azadeh,Sayahpour Forough A.,Amiri Parvin,Larijani Bagher,Amoli Mahsa M.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03256435.pdf

Reference31 articles.

1. Sperling MA. ATP-sensitive potassium channels: neonatal diabetes mellitus and beyond. N Engl J Med 2006 Aug 3; 355(5): 507–10

2. Sperling MA. Neonatal diabetes mellitus: from understudy to center stage. Curr Opin Pediatr 2005 Aug; 17(4): 512–8

3. Slingerland AS, Shields BM, Flanagan SE, et al. Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births. Diabetologia 2009 Aug; 52(8): 1683–5

4. Iafusco D, Massa O, Pasquino B, et al. Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births. Acta Diabetol. Epub 2011 Sep 28

5. Polak M, Shield J. Neonatal and very-early-onset diabetes mellitus. Semin Neonatol 2004 Feb; 9(1): 59–65

Cited by 6 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. Independent case-control study in KCNJ11 gene polymorphism with Type 2 diabetes Mellitus;Saudi Journal of Biological Sciences;2022-04

2. Genetic research in Immunogenetics Group of Endocrinology and Metabolism Research Institute;Journal of Diabetes & Metabolic Disorders;2021-02-15

3. Monogenic Causes in the Type 1 Diabetes Genetics Consortium Cohort: Low Genetic Risk for Autoimmunity in Case Selection;The Journal of Clinical Endocrinology & Metabolism;2021-02-04

4. Transient neonatal diabetes mellitus and activating mutation in the KCNJ11 gene in two siblings;Archives de Pédiatrie;2017-05

5. Transient neonatal diabetes due to a missense mutation (E227K) in the gene encoding the ATP ‐sensitive potassium channel ( KCNJ 11);Clinical Case Reports;2015-08-26

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