Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema
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| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2025-02-01
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| Series: | Orphanet Journal of Rare Diseases |
| Online Access: | https://doi.org/10.1186/s13023-025-03572-z |
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| _version_ | 1823861663253659648 |
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| author | Lingxi Jiang Chao Dai Suyang Duan Tingting Wang Chunbao Xie Luhan Zhang Zimeng Ye Xiumei Ma Yi Shi |
| author_facet | Lingxi Jiang Chao Dai Suyang Duan Tingting Wang Chunbao Xie Luhan Zhang Zimeng Ye Xiumei Ma Yi Shi |
| author_sort | Lingxi Jiang |
| collection | DOAJ |
| format | Article |
| id | doaj-art-9cd1c73a276249329b9bcb675412e614 |
| institution | Kabale University |
| issn | 1750-1172 |
| language | English |
| publishDate | 2025-02-01 |
| publisher | BMC |
| record_format | Article |
| series | Orphanet Journal of Rare Diseases |
| spelling | doaj-art-9cd1c73a276249329b9bcb675412e6142025-02-09T12:54:06ZengBMCOrphanet Journal of Rare Diseases1750-11722025-02-012011210.1186/s13023-025-03572-zCorrection To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedemaLingxi Jiang0Chao Dai1Suyang Duan2Tingting Wang3Chunbao Xie4Luhan Zhang5Zimeng Ye6Xiumei Ma7Yi Shi8Sichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaSchool of Medicine, University of SydneySichuan Provincial Key Laboratory for Human Disease Gene Study and the Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People’s, Hospital, University of Electronic Science and Technology of ChinaDepartment of Ophthalmology, Sichuan Provincial People’s Hospital, University of Electronic Science and Technology of Chinahttps://doi.org/10.1186/s13023-025-03572-z |
| spellingShingle | Lingxi Jiang Chao Dai Suyang Duan Tingting Wang Chunbao Xie Luhan Zhang Zimeng Ye Xiumei Ma Yi Shi Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema Orphanet Journal of Rare Diseases |
| title | Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema |
| title_full | Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema |
| title_fullStr | Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema |
| title_full_unstemmed | Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema |
| title_short | Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema |
| title_sort | correction to uncovering a novel serping1 pathogenic variant insights into the aggregation of c1 inh in hereditary angioedema |
| url | https://doi.org/10.1186/s13023-025-03572-z |
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