Genetic variants of ABCC8 and phenotypic features in Chinese early onset diabetes-Reference-Cited by-同舟云学术

Genetic variants of ABCC8 and phenotypic features in Chinese early onset diabetes

Published:2021-01-04 Issue:7 Volume:13 Page:542-553
ISSN:1753-0393
Container-title:Journal of Diabetes
language:en
Short-container-title:Journal of Diabetes

Author:

Li Meng¹^ORCID,Gong Siqian¹,Han Xueyao¹,Zhang Simin¹,Ren Qian¹,Cai Xiaoling¹,Luo Yingying¹,Zhou Lingli¹,Zhang Rui¹^ORCID,Liu Wei¹,Zhu Yu¹,Zhou Xianghai¹,Sun Yanfang²,Li Yufeng³,MA Yumin¹,Ji Linong¹^ORCID

Affiliation:

1. Department of Endocrinology and Metabolism Peking University People's Hospital, Peking University Diabetes Center Beijing China

2. Department of Internal Medicine Hebei Province Sanhe Hospital Langfang China

3. Department of Endocrinology and Metabolism Capital Medical University Pinggu Hospital Beijing China

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1753-0407.13144

Reference47 articles.

1. Maturity-onset diabetes of the young (MODY): an update

2. Systematic Population Screening, Using Biomarkers and Genetic Testing, Identifies 2.5% of the U.K. Pediatric Diabetes Population With Monogenic Diabetes

3. Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor;Inagaki N;Science (New York, NY),1995

4. Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATPchannel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period

5. Heterozygous ABCC8 mutations are a cause of MODY

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