Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB , and FGG genes
Year: 2025
Type: article
Study design: Case Report
Source: Laboratory Medicine
Authors: Yangyang Wu, Kaili Qin, Liqun Xiang, Meiling Luo, Min Chen, Xinyan Chen, Jie Yan, Weijie Zhou, Faquan Lin, Lin Liao
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W4416227139
