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Article

Two novel mutations at contiguous codons in the fibrinogen Bbeta chain associated with hypofibrinogenaemia.

Thrombosis and haemostasis - 1 May 2009

Davis Ryan L, May Stephen, Chunilal Sanjeev, Brennan Stephen O

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

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PMID: 19404555

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Two novel mutations at contiguous codons in the fibrinogen Bbeta chain associated with hypofibrinogenaemia.PMID 19404555Read ↗

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Hypofibrinogenemia in an individual with 2 coding (gamma82 A-->G and Bbeta235 P-->L) and 2 noncoding mutations.Semantic proximity Read ↗

Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy.Semantic proximity Read ↗

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Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.Semantic proximity Read ↗

Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil.Semantic proximity Read ↗

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Familial hypofibrinogenaemia associated with heterozygous substitution of a conserved arginine residue; Bbeta255 Arg-->His (Fibrinogen Merivale).Semantic proximity Read ↗

A Bbeta 14 Arg --> Cys fibrinogen variant in a patient with thrombotic complications (fibrinogen St-Germain III).Semantic proximity Read ↗

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