等位基因
疾病
医学
风险因素
肝细胞
内科学
遗传学
生物
基因
体外
作者
Chaochao Yang,Linong Ji,X. Y. Han
标识
DOI:10.1210/clinem/dgae602
摘要
Rare variants in HNF1A cause both maturity onset diabetes of the young 3 (HNF1A-MODY) and reduced serum C reactive protein (CRP) levels. Common variants of HNF1A are associated with serum CRP and type 2 diabetes, but inconsistently with cardiovascular disease (CVD).
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