Literature DB >> 3091610

The molecular genetics of haemophilia A and B.

G G Brownlee.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1986        PMID： 3091610     DOI： 10.1242/jcs.1986.supplement_4.24

Source DB:  PubMed          Journal:  J Cell Sci Suppl        ISSN： 0269-3518


× No keyword cloud information.
  4 in total

1.  Hemophilia B (factor IXSeattle 2) due to a single nucleotide deletion in the gene for factor IX.

Authors:  B G Schach; S Yoshitake; E W Davie
Journal:  J Clin Invest       Date:  1987-10       Impact factor: 14.808

2.  The propeptide region of clotting factor IX is a signal for a vitamin K dependent carboxylase: evidence from protein engineering of amino acid -4.

Authors:  P Galeffi; G G Brownlee
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

3.  Factor IXMadrid 2: a deletion/insertion in factor IX gene which abolishes the sequence of the donor junction at the exon IV-intron d splice site.

Authors:  J Solera; M Magallón; J Martin-Villar; A Coloma
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

4.  Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.

Authors:  M Ludwig; R Schwaab; A Eigel; J Horst; H Egli; H H Brackmann; K Olek
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.