𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular characterization of the ERGIC-53 gene in two Japanese patients with combined factor V–factor VIII deficiency

✍ Scribed by H. Dansako; F. Ishimaru; Y. Takai; J. Tomoda; K. Nakase; K. Fujii; Y. Ogama; T. Kozuka; N. Sezaki; K. Honda; M. Harada


Publisher
Springer
Year
2001
Tongue
English
Weight
46 KB
Volume
80
Category
Article
ISSN
0939-5555

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Molecular diagnostics of 15 hemophilia A
✍ Kamiab Tavassoli; Antonin Eigel; Klaus Wilke; Hartmut Pollmann; Jürgen Horst 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 130 KB 👁 2 views

The X-linked bleeding disorder hemophilia A is caused by mutations in the coagulation factor VIII gene. A high frequency of de novo mutations and the large size of this gene complicate the molecular diagnostic of hemophilia A. Characterization of mutations, however, may help identify amino acids or

Role of the 2 adenine (g.11293_11294insA
✍ F. Peyvandi; I. Garagiola; R. Palla; N. Marziliano; P. M. Mannucci 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 330 KB 👁 1 views

Polymorphic variants in the gene encoding factor VII (F7) affect the plasma levels of this coagulation protein and modify the clinical phenotype of FVII deficiency in some patients. In this study we report the in vitro functional analysis of a novel polymorphic variant located in the 3 0 untranslate