Article Information
History
- January 30, 2020.
Copyright
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Author Information
- Aiqiu Wei1,#,
- Yangyang Wu1,#,
- Liqun Xiang1,
- Jie Yan1,
- Peng Cheng2,
- Donghong Deng2,* and
- Faquan Lin1,*
- 1Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China
- 2Department of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China
- ↵*Corresponding authors: Faquan Lin, Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China. Email: fqlin1998{at}163.com. Donghong Deng, Department of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China. Email: ddh_gx{at}163.com.
↵# Aiqiu Wei and Yangyang Wu contributed equally to this work and are co-first authors.
Posted January 30, 2020.
A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia
