GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patients-Reference-Cited by-同舟云学术

GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patients

Published:2021-05-04 Issue:6 Volume:19 Page:1412-1424
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Ghosh Suvoshree¹,Kraus Katrin¹,Biswas Arijit¹,Müller Jens¹,Buhl Anna‐Lena¹,Forin Francesco¹,Singer Heike¹,Höning Klara²,Hornung Veit²³,Watzka Matthias¹⁴,Czogalla‐Nitsche Katrin J.¹,Oldenburg Johannes¹⁴

Affiliation:

1. Institute of Experimental Haematology and Transfusion Medicine University Clinic Bonn Bonn Germany

2. Institute for Clinical Chemistry and Clinical Pharmacology Unit for Clinical Biochemistry University HospitalUniversity of Bonn Bonn Germany

3. GeneCenter and Department of Biochemistry Ludwig‐Maximilians‐Universität München Munich Germany

4. Center for Rare Diseases Bonn University Clinic Bonn Bonn Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.15238

Reference45 articles.

1. The Vitamin K–Dependent Carboxylase

2. Vitamin K-dependent carboxylation of the carboxylase

3. Vitamin K Oxygenation, Glutamate Carboxylation, and Processivity: Defining the Three Critical Facets of Catalysis by the Vitamin K–Dependent Carboxylase

4. γ-carboxyglutamate-containing proteins and the vitamin K-dependent carboxylase

5. Characterization of the complementary deoxyribonucleic acid and gene coding for human prothrombin

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