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. Int. J. Mol. Sci. 2017, 18, 2470.
https://doi.org/10.3390/ijms18112470
AMA Style
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
Chicago/Turabian Style
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
APA Style
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