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Taira C, Matsuda K, Arai S, Sugano M, Uehara T, Okumura N. 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. International Journal of Molecular Sciences. 2017; 18(11):2470. https://doi.org/10.3390/ijms18112470

Taira, Chiaki, Kazuyuki Matsuda, Shinpei Arai, Mitsutoshi Sugano, Takeshi Uehara, and Nobuo Okumura. 2017. "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" International Journal of Molecular Sciences 18, no. 11: 2470. https://doi.org/10.3390/ijms18112470

Taira, C., Matsuda, K., Arai, S., Sugano, M., Uehara, T., & Okumura, N. (2017). 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. International Journal of Molecular Sciences, 18(11), 2470. https://doi.org/10.3390/ijms18112470