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A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and arterial thrombosis
Shlebak, Abdul A., Katsarou, Alexia D., Adams, George, Fernando, FionaLanguage:
english
Journal:
Journal of Thrombosis and Thrombolysis
DOI:
10.1007/s11239-016-1439-z
Date:
November, 2016
File:
PDF, 512 KB
english, 2016