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A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations.

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Bibliographic Details
Title: A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations.
Authors: Chen, Wanling1 (AUTHOR), Hu, Jiasheng2 (AUTHOR) xdzsxmmc@126.com
Source: Thrombosis Journal. 6/12/2025, Vol. 23 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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ISSN:14779560
DOI:10.1186/s12959-025-00746-4