Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema
Saved in:
Main Authors: | Lingxi Jiang, Chao Dai, Suyang Duan, Tingting Wang, Chunbao Xie, Luhan Zhang, Zimeng Ye, Xiumei Ma, Yi Shi |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2025-02-01
|
Series: | Orphanet Journal of Rare Diseases |
Online Access: | https://doi.org/10.1186/s13023-025-03572-z |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema
by: Lingxi Jiang, et al.
Published: (2024-09-01) -
Hereditary angioedema diagnosis evaluation score (HADES): A new clinical scoring system for predicting hereditary angioedema with C1 inhibitor deficiency
by: Ricardo Zwiener, MD, et al.
Published: (2025-05-01) -
De Novo or inherited: gonosomal mosaicism in hereditary angioedema due to C1 inhibitor deficiency
by: Laura Batlle-Masó, et al.
Published: (2025-02-01) -
Vasculopathy: a possible factor affecting hereditary angioedema
by: Anna Laura Colia, et al.
Published: (2025-02-01) -
Hereditary Angioedema and Gastrointestinal Complications: An Extensive Review of the Literature
by: Napoleon Patel, et al.
Published: (2015-01-01)