HBA2 : C.4delG: A Novel Frameshift Mutation Causing α + -Thalassemia Found in a Chinese Family
Year: 2025
Type: article
Study design: Case Report
Source: Hemoglobin
Authors: Wei Li, Guixi Wei, Shan Ren, Zulin Xie, Xuan Luo, Lanzuo Zhang, Yuanyuan Huang, Dejian Yuan
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W4412095289
