Identification and functional analysis of GCK gene mutations in 12 Chinese families with hyperglycemia.
Zhixin WangChengming DiaoYijing LiuMingmin LiJia ZhengQian ZhangMiao YuHuabing ZhangFan PingMing LiXinhua XiaoPublished in: Journal of diabetes investigation (2019)
We have identified 11 GCK mutations and one variant of uncertain significance in 12 Chinese families with hyperglycemia. For five GCK mutations (R43C, K169N, R191W, E221K and A379E), the changes in enzyme kinetics and thermostability might be the pathogenic mechanisms by which mutations cause hyperglycemia.
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