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Article

Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 May 2008

Castaman G, Giacomelli S H, Duga S, Rodeghiero F

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Share to Afibrinogenemia
Share to Blood Coagulation Tests
Share to Codon, Nonsense
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibrinogen

Share to Fibrinogens, Abnormal

Share to Mutation, Missense

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Identifiers

PMID: 18393984
DOI: 10.1111/j.1365-2516.2008.01692.x

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