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Journal Articles

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine–based ER retention motif

Katrin J. Czogalla, Arijit Biswas, Simone Rost, Matthias Watzka, Johannes Oldenburg
Journal: Blood
Blood (2014) 124 (8): 1354–1362.
https://doi.org/10.1182/blood-2013-12-545988
Published: 2014
Includes: Supplemental data
Journal Articles

Mutations in the VKORC1 Gene Cause Warfarin Resistance, Warfarin Sensitivity and Combined Deficiency of Vitamin K Dependent Coagulation Factors.

Johannes Oldenburg, MD, PhD, Simone Rost, Andreas Fregin, PhD, Christof Geisen, Vytautas Ivaskevicius, MD, Erhard Seifried, MD, Inge Scharrer, MD, Maximilian Heistinger, MD, Edward Tuddenham, MD, Clemens Muller-Reible, PhD, Barbara Zieger, MD
Journal: Blood
Blood (2004) 104 (11): 277.
https://doi.org/10.1182/blood.V104.11.277.277
Published: 2004
Journal Articles

Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16

Andreas Fregin, Simone Rost, Werner Wolz, Alice Krebsova, Clemens R. Muller, Johannes Oldenburg
Journal: Blood
Blood (2002) 100 (9): 3229–3232.
https://doi.org/10.1182/blood-2002-03-0698
Published: 2002
Journal Articles

De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism

Brief Report
Johannes Oldenburg, Simone Rost, Osman El-Maarri, Marco Leuer, Klaus Olek, Clemens R. Müller, Rainer Schwaab
Journal: Blood
Blood (2000) 96 (8): 2905–2906.
https://doi.org/10.1182/blood.V96.8.2905
Published: 2000