MODY2 in Asia: analysis of GCK mutations and clinical characteristics

Zhou, Y; Wang, SN; Wu, J; Dong, JJ; Liao, L

Liao, L (corresponding author), Shandong First Med Univ, Dept Endocrinol & Metabol, Affiliated Hosp 1, Jinan, Peoples R China.; Dong, JJ (corresponding author), Shandong Univ, Dept Endocrinol, Qilu Hosp, Jinan, Peoples R China.; Liao, L (corresponding author), Shandong Univ, Shandong Prov Qianfoshan Hosp, Cheeloo Coll Med, Dept Endocrinol & Metabol, Jinan, Peoples R China.

ENDOCRINE CONNECTIONS, 2020; 9 (5): 471

Abstract

Aims: Heterozygous inactivating mutations in the GCK gene cause the familial, mild fasting hyperglycaemia named MODY2. Many patients with MODY2 in Asi......

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