Literature DB >> 27710858

Novel FGB mutation Bβ240Cys→Arg confirms importance of the Bβ211-240 disulphide for plasma expression of fibrinogen.

Stephen O Brennan1, Andrew D Laurie2, Julie-Anne Bell3.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27710858     DOI: 10.1016/j.thromres.2016.09.031

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


× No keyword cloud information.
  1 in total

1.  A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia.

Authors:  Chiaki Taira; Kazuyuki Matsuda; Shinpei Arai; Mitsutoshi Sugano; Takeshi Uehara; Nobuo Okumura
Journal:  Int J Mol Sci       Date:  2017-11-20       Impact factor: 5.923

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.