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Journal: Int. J. Mol. Sci., 2017
Volume: 18
Number: 2470

Article: A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia
Authors: by , , , , and
Link: https://www.mdpi.com/1422-0067/18/11/2470

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