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A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia

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Description scientific article published on December 23, 2012
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author: Steve Brennan 

Publication date December 23, 2012
Language English
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https://api.elsevier.com/content/article/PII:S107997961200229X?httpAccept=text/xml

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