NEUROD1‐deficient diabetes ( MODY6 ): Identification of the first cases in Japanese and the clinical features-Reference-Cited by-同舟云学术

NEUROD1‐deficient diabetes ( MODY6 ): Identification of the first cases in Japanese and the clinical features

Published:2017-06-30 Issue:2 Volume:19 Page:236-242
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Horikawa Yukio¹²^ORCID,Enya Mayumi¹²,Mabe Hiroyo³,Fukushima Kei⁴,Takubo Noriyuki⁴,Ohashi Masaaki⁵,Ikeda Fuki⁶,Hashimoto Ken‐ichi¹²,Watada Hirotaka⁶,Takeda Jun¹²

Affiliation:

1. Department of Diabetes and Endocrinology Gifu University Graduate School of Medicine Gifu Japan

2. Division of Clinical Genetics Gifu University Hospital Gifu Japan

3. Department of Child Development Kumamoto University Hospital Kumamoto Japan

4. Department of Pediatrics Juntendo University Hospital Tokyo Japan

5. Department of Diabetes and Endocrinology Saku Central Hospital Nagano Japan

6. Department of Metabolism & Endocrinology Juntendo University Graduate School of Medicine Tokyo Japan

Funder

Japan Science and Technology Agency

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pedi.12553

Reference22 articles.

1. Molecular Mechanisms and Clinical Pathophysiology of Maturity-Onset Diabetes of the Young

2. Exome Sequencing and Genetic Testing for MODY

3. Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor.

4. Transactivation of the Mouse Sulfonylurea Receptor I Gene by BETA2/NeuroD

5. BETA2 Activates Transcription From the Upstream Glucokinase Gene Promoter in Islet β-Cells and Gut Endocrine Cells

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