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Journal Abstract Search

149 related items for PubMed ID: 31259773

  • 1. Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.
    Zhang H, Luo S, Fang W, Liu S, Su K, Yang L, Jin Y, Wang M.
    Blood Coagul Fibrinolysis; 2019 Jul; 30(5):233-238. PubMed ID: 31259773
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  • 2. A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia.
    Jia K, Zeng M, Zheng X, Xie H, Yang L, Xie Y, Wang M.
    Hamostaseologie; 2023 Dec; 43(6):426-431. PubMed ID: 37516116
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  • 3. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
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  • 7. [Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].
    Zhu L, Zhao M, Cheng X, Yu D, Li X, Xu F, Wang J, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):179-183. PubMed ID: 29652987
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  • 8. Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
    Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M.
    Blood; 2003 Dec 15; 102(13):4413-5. PubMed ID: 12893758
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  • 10. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
    Fang Y, Wang HL, Wang XF, Fu QH, Wang WB, Xie S, Zhou RF, Dai J, Wang ZY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec 15; 13(6):1086-9. PubMed ID: 16403286
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  • 11. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
    Simurda T, Zolkova J, Snahnicanova Z, Loderer D, Skornova I, Sokol J, Hudecek J, Stasko J, Lasabova Z, Kubisz P.
    Int J Mol Sci; 2017 Dec 29; 19(1):. PubMed ID: 29286337
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  • 13. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 29; 34(9):751-6. PubMed ID: 24103871
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  • 14. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.
    Casini A, Lukowski S, Quintard VL, Crutu A, Zak M, Regazzoni S, de Moerloose P, Neerman-Arbez M.
    Thromb Res; 2014 May 29; 133(5):868-74. PubMed ID: 24560896
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  • 15. [Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].
    Jia KQ, Su ZX, Chen HL, Zheng XY, Zeng ML, Zhang K, Ye LY, Yang LL, Jin YH, Wang MS.
    Zhonghua Xue Ye Xue Za Zhi; 2023 Nov 14; 44(11):930-935. PubMed ID: 38185523
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  • 16. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
    Xu XC, Zhou RF, Wu JS, Fang Y, Wang XF, Zhai ZM, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar 14; 26(3):137-9. PubMed ID: 15946523
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  • 19. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M, Leinoe E, Rossing M, Norström E, Zetterberg E.
    Blood Coagul Fibrinolysis; 2020 Oct 14; 31(7):481-484. PubMed ID: 32852326
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  • 20. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
    Xue F, Ge J, Gu DS, DU WT, Sui T, Zhao HF, Zhang L, Yang RC.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug 14; 17(4):1021-5. PubMed ID: 19698251
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