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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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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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  Data: A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations.
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  Data: <searchLink fieldCode="AR" term="%22Chen%2C+Wanling%22">Chen, Wanling</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hu%2C+Jiasheng%22">Hu, Jiasheng</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> xdzsxmmc@126.com</i>
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  Data: <searchLink fieldCode="JN" term="%22Thrombosis+Journal%22">Thrombosis Journal</searchLink>. 6/12/2025, Vol. 23 Issue 1, p1-7. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=185942015
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        Value: 10.1186/s12959-025-00746-4
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        Text: English
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      – TitleFull: A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations.
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            NameFull: Chen, Wanling
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            NameFull: Hu, Jiasheng
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              Text: 6/12/2025
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              Y: 2025
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