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VKORC1 ER mislocalization causes rare disease
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).(1)
Gorde:
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Society of Hematology
2014
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| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4141510/ https://ncbi.nlm.nih.gov/pubmed/25147380 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-07-586032 |
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