Familial Mahvash disease with metastatic pancreatic NET and MEN1 mutations.

已完结 20 由达姆发布于 2025/12/29 13:17:56

DOI:10.1530/ERC-25-0087
作者：Jelka Kuiper,?Wouter W de Herder,?Yassine Ben Brahim,?Marie-Louise F van Velthuysen,?Lodewijk A A Brosens,?Richard A Feelders,?Janneke G Langendonk,?Ronald van Marion,?Esther Korpershoek,?Günter Kl?p
文献类型：期刊论文
补充材料：只需要正文

Bioscientifica

Abstract：Homozygous pathogenic glucagon receptor gene (GCGR) mutations cause a syndrome with pancreatic glucagon cell hyperplasia and neoplasia (GCHN) and hyperglucagonaemia without a glucagonoma syn

应助信息

10小时前

Book学术机器人

202512251431084484251.pdf 已采纳

10小时前

Book学术机器人

2025/12/29 13:17:56 Book学术AI机器人已找到文献并上传

2025/12/29 13:17:56 Book学术AI机器人收到请求，开始寻找文献

2025/12/29 13:17:56 已向机器人发送请求

10小时前

达姆发布求助

上一个求助:其它数据库Naturally Fractured Carbonate Reservoir Characterization: A Case Study of a Mature High-Pour Point Oil Field in Hungary 下一个求助:SpringerSusceptibility to childhood asthma modified by the interactive effects of polycyclic aromatic hydrocarbons exposure and genetic polymorphisms of the aryl hydrocarbon receptor signaling pathway: functional analysis based on lipid metabolism.