MODY2 in Asia: analysis of GCK mutations and clinical characteristics

AIMS: Heterozygous inactivating mutations in the GCK gene cause the familial, mild fasting hyperglycaemia named MODY2. Many patients with MODY2 in Asia have delayed timely treatment because they did not receive the correct diagnosis. This study aims to analyze the clinical characteristics and GCK mu...

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Detalles Bibliográficos
Autores principales: Zhou, Yuan, Wang, ShengNan, Wu, Jing, Dong, JianJun, Liao, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274558/
https://www.ncbi.nlm.nih.gov/pubmed/32375122
http://dx.doi.org/10.1530/EC-20-0074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274558/
https://www.ncbi.nlm.nih.gov/pubmed/32375122
http://dx.doi.org/10.1530/EC-20-0074

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