Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens-Reference-Cited by-同舟云学术

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Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens

Published:2020-01-20 Issue:2 Volume:42 Page:190-197
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Kaido Takahiro¹,Yoda Masahiro¹,Kamijo Tomu¹,Taira Chiaki¹,Higuchi Yumiko¹,Okumura Nobuo¹^ORCID

Affiliation:

1. Department of Clinical Laboratory Investigation Graduate School of Medicine Shinshu University Matsumoto Japan

Funder

Japan Society for the Promotion of Sicences KAKENHI

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13152

Reference22 articles.

1. Fibrinogen and Fibrin

2. The Role of βγ and αγ Complexes in the Assembly of Human Fibrinogen

3. Recommendations for nomenclature on fibrinogen and fibrin

4. Fibrinogen and fibrin structure and functions

5. FIBRINOGEN AND FIBRIN

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1. A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype;Hereditas;2024-01-18

2. Development and validation of a nomogram for ISR within 2 years in patients after iliac or femoral artery stent placement;2023-07-31

3. The clinical significance of serum HMGB1 in patients with lower extremity arteriosclerosis obliterans after interventional vascular restenosis;Frontiers in Surgery;2023-01-06

4. Pediatric patient with fibrinogen Villeurbanne II presenting with an unprovoked portal vein thrombosis;Blood Advances;2022-07-22

5. Mutations Accounting for Congenital Fibrinogen Disorders: An Update;Seminars in Thrombosis and Hemostasis;2022-01-24

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