医学
听力损失
基因型
疾病
听力学
皮肤病科
表型
病理
遗传学
生物
基因
作者
Bingxuan Wu,Yuanyuan Luo,Di Wu,Yi Wang,Min Shen
出处
期刊:Rheumatology
[Oxford University Press]
日期:2023-09-01
卷期号:63 (6): 1690-1698
被引量:1
标识
DOI:10.1093/rheumatology/kead451
摘要
Nucleotide-binding oligomerization domain-like receptor family, pyrin domain containing 3-associated autoinflammatory disease (NLRP3-AID) is a rare autosomal dominant systemic autoinflammatory disease. We aimed to summarize the phenotypic and genotypic features of Chinese adult NLRP3-AID patients with hearing loss.
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