Orphanet journal of rare diseases
Novel compound heterozygous mutations in plasminogen (p.Gly568Arg/p.Ala620Thr) impair protein structure and function in type II deficiency: mechanistic insights into a hereditary thrombogenic disorder.
Yifan Lu, Fengjiao Wang, Dandan Yu, Haixiao Xie, Yanhui Jin, Mingshan Wang, Lihong Yang
Published: 202510.1186/s13023-025-04122-3
No abstract available for this study.