The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif.
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Structural Modeling Insights into Human VKORC1 PhenotypesVKORC1 and VKORC1L1: Why do Vertebrates Have Two Vitamin K 2,3-Epoxide Reductases?Structural and functional insights into enzymes of the vitamin K cycleARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis.GGCX and VKORC1 inhibit osteocalcin endocrine functions.Membrane Cholesterol Modulates Superwarfarin Toxicity.VKORC1 ER mislocalization causes rare disease.Vitamin K epoxide reductase and its paralogous enzyme have different structures and functions.
P2860
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P2860
The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif.
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The Arg98Trp mutation in human ...... nine-based ER retention motif.
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type
label
The Arg98Trp mutation in human ...... nine-based ER retention motif.
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prefLabel
The Arg98Trp mutation in human ...... nine-based ER retention motif.
@en
P2093
P1433
P1476
The Arg98Trp mutation in human ...... nine-based ER retention motif.
@en
P2093
Johannes Oldenburg
Katrin J Czogalla
Matthias Watzka
Simone Rost
P304
P356
10.1182/BLOOD-2013-12-545988
P407
P577
2014-06-24T00:00:00Z