2024-03-29T04:45:15Z
https://soar-ir.repo.nii.ac.jp/oai
oai:soar-ir.repo.nii.ac.jp:02000564
2022-12-14T04:23:47Z
461:462
Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative
Yoda, Masahiro
Kaido, Takahiro
Taira, Chiaki
Higuchi, yumiko
Arai, Shinpei
Okumura, Nobuo
hypodysfibrinogenemia
splicing abnormality
FGB
nonsense-mediated mRNA decay
fibrin polymerization
Article
Thrombosis research. 196: 152-158. (2020)
journal article
Pergamon Press
2020-12
application/pdf
Thrombosis research
196
152
158
1879-2472
https://soar-ir.repo.nii.ac.jp/record/2000564/files/ThrombRes196_152.pdf
eng
32871307
https://pubmed.ncbi.nlm.nih.gov/32871307/
10.1016/j.thromres.2020.08.031
https://doi.org/10.1016/j.thromres.2020.08.031