In this issue of Blood, Czogalla et al identify that the rare heritable hemorrhaging disease, vitamin K-dependent clotting factor deficiency type 2 (VKCFD2), is caused by mislocalization of vitamin K epoxide reductase (VKORC1) in the endoplasmic reticulum (ER).
|Original language||English (US)|
|Number of pages||2|
|State||Published - Aug 21 2014|
ASJC Scopus subject areas
- Cell Biology