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Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype.

Pediatric blood & cancer - 1 Mar 2021

Abdelghani Eman, Dawson Jennifer, Zajo Kristin, Hallam Michelle, Dunn Amy, Kumar Riten

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 33058516
DOI: 10.1002/pbc.28713

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Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype.PMID 33058516Read ↗

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A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding PhenotypeSemantic proximity Read ↗

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