A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype ; volume:161 ; number:1 ; day:18 ; month:1 ; year:2024 ; pages:1-9 ; date:12.2024
Hereditas ; 161, Heft 1 (18.1.2024), 1-9, 12.2024
- Creator
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Xu, Nuo
Zheng, Liping
Dai, Zhehao
Zhu, Jun
Xie, Peng
Yang, Shun
Chen, Fei
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s41065-024-00308-0
- URN
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urn:nbn:de:101:1-2024033110123798603536
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:49 AM CEST
Data provider
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Associated
- Xu, Nuo
- Zheng, Liping
- Dai, Zhehao
- Zhu, Jun
- Xie, Peng
- Yang, Shun
- Chen, Fei
- SpringerLink (Online service)
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