2024-03-28T13:34:38Z
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)
Pergamon Press
2020-12
eng
journal article
AM
http://hdl.handle.net/10091/0002000564
https://soar-ir.repo.nii.ac.jp/records/2000564
https://pubmed.ncbi.nlm.nih.gov/32871307/
32871307
https://doi.org/10.1016/j.thromres.2020.08.031
10.1016/j.thromres.2020.08.031
1879-2472
Thrombosis research
196
152
158
https://soar-ir.repo.nii.ac.jp/record/2000564/files/ThrombRes196_152.pdf
application/pdf
2022-01-04