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3. Two novel mutations in the fibrinogen γ nodule. Kotlín R; Pastva O; Stikarová J; Hlaváčková A; Suttnar J; Chrastinová L; Riedel T; Salaj P; Dyr JE Thromb Res; 2014 Oct; 134(4):901-8. PubMed ID: 25074738 [TBL] [Abstract][Full Text] [Related]
4. Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens. Kaido T; Yoda M; Kamijo T; Taira C; Higuchi Y; Okumura N Int J Lab Hematol; 2020 Apr; 42(2):190-197. PubMed ID: 31957968 [TBL] [Abstract][Full Text] [Related]
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7. A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release. Yan J; Luo M; Cheng P; Liao L; Deng X; Deng D; Lin F Int J Hematol; 2017 Apr; 105(4):506-514. PubMed ID: 27933517 [TBL] [Abstract][Full Text] [Related]
8. Decreased lateral aggregation of a variant recombinant fibrinogen provides insight into the polymerization mechanism. Mullin JL; Gorkun OV; Lord ST Biochemistry; 2000 Aug; 39(32):9843-9. PubMed ID: 10933802 [TBL] [Abstract][Full Text] [Related]
9. Differences in the function and secretion of congenital aberrant fibrinogenemia between heterozygous γD320G (Okayama II) and γΔN319-ΔD320 (Otsu I). Mukai S; Ikeda M; Takezawa Y; Sugano M; Honda T; Okumura N Thromb Res; 2015 Dec; 136(6):1318-24. PubMed ID: 26573395 [TBL] [Abstract][Full Text] [Related]
10. Fibrinogen St. Gallen I (gamma 292 Gly--> Val): evidence for structural alterations causing defective polymerization and fibrinogenolysis. Stucki B; Schmutz P; Schmid L; Haeberli A; Lämmle B; Furlan M Thromb Haemost; 1999 Feb; 81(2):268-74. PubMed ID: 10064005 [TBL] [Abstract][Full Text] [Related]
12. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His. Luo M; Deng D; Xiang L; Cheng P; Liao L; Deng X; Yan J; Lin F Medicine (Baltimore); 2016 Sep; 95(39):e4864. PubMed ID: 27684817 [TBL] [Abstract][Full Text] [Related]
13. Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a". Lounes KC; Soria C; Mirshahi SS; Desvignes P; Mirshahi M; Bertrand O; Bonnet P; Koopman J; Soria J Blood; 2000 Nov; 96(10):3473-9. PubMed ID: 11071644 [TBL] [Abstract][Full Text] [Related]
14. A novel fibrinogen variant (fibrinogen Seoul II; AalphaGln328Pro) characterized by impaired fibrin alpha-chain cross-linking. Park R; Doh HJ; An SS; Choi JR; Chung KH; Song KS Blood; 2006 Sep; 108(6):1919-24. PubMed ID: 16735602 [TBL] [Abstract][Full Text] [Related]
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19. A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization. Koopman J; Haverkate F; Briët E; Lord ST J Biol Chem; 1991 Jul; 266(20):13456-61. PubMed ID: 2071611 [TBL] [Abstract][Full Text] [Related]
20. Congenital hypodysfibrinogenemia associated with a novel deletion of three residues (γAla289_Asp291del) in fibrinogen. Zhu L; Zhao M; Wang M; Lou Z; Chen X; Pan L; Yu D; Xia W; Wang H; Zhou B; Gao S J Thromb Thrombolysis; 2018 Aug; 46(2):211-218. PubMed ID: 29748775 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]