fibrinogen beta chain isoform 3 preproprotein [Homo sapiens]

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A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia. [Hamostaseologie. 2023]
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. Epub 2023 Jul 29.
Association between fibrinogen level and length of stay in patients with lower extremity atherosclerotic disease: a retrospective cohort study. [Sci Rep. 2023]
Association between fibrinogen level and length of stay in patients with lower extremity atherosclerotic disease: a retrospective cohort study.
Wang X, Yang Y, Yu L, Pang C, Sun W, Zang S, Li C. Sci Rep. 2023 Jul 22; 13(1):11872. Epub 2023 Jul 22.
Pathogenic Role of Fibrinogen in the Neuropathology of Multiple Sclerosis: A Tale of Sorrows and Fears. [Neurochem Res. 2023]
Pathogenic Role of Fibrinogen in the Neuropathology of Multiple Sclerosis: A Tale of Sorrows and Fears.
Alruwaili M, Al-Kuraishy HM, Alexiou A, Papadakis M, ALRashdi BM, Elhussieny O, Saad HM, Batiha GE. Neurochem Res. 2023 Nov; 48(11):3255-3269. Epub 2023 Jul 13.

RefSeq genomic sequence
See the genomic reference sequence for the FGB gene (NG_008833.1).
RefSeq mRNA
See reference mRNA sequence for the FGB gene (NM_001382759.1).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the FGB gene.

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Protein