Hereditary protein C deficiency caused by the compound heterozygous mutations, Gly 282 Ser and Met 364 Ile ; Contribution of each protein C mutation on pathogenesis of thrombosis-Reference-Cited by-同舟云学术

Hereditary protein C deficiency caused by the compound heterozygous mutations, Gly 282 Ser and Met 364 Ile ; Contribution of each protein C mutation on pathogenesis of thrombosis

Published:2011 Issue:3 Volume:22 Page:87-99
ISSN:0915-7441
Container-title:Japanese Journal of Thrombosis and Hemostasis
language:en
Short-container-title:Nihon Kessen Shiketsu Gakkaishi

Author:

YUI Tomoo¹,OCHI Morio¹,TAKAHASHI Nobuhiko²,IEKO Masahiro²,HAYASHI Tatsuya³,SUZUKI Koji⁴

Affiliation:

1. Division of Fixed Prosthodontics and Oral Implantrology, Department of Oral Rehabilitation

2. Department of Internal Medicine, School of Dentistry, Health Sciences University of Hokkaido

3. Department of Biochemistry, School of Nursing, Mie Prefectural College of Nursing

4. Department of Molecular Pathobiology, Mie University Graduate School of Medicine

Publisher

Japanese Society on Thrombosis and Hemostasis

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/jjsth/22/3/22_3_87/_pdf

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2. 2) Dahlback B, Villoutreix BO : Regulation of blood coagulation by the protein C anticoagulant pathway : novel insights into structure-function relationships and molecular recognition. Arterioscler Thromb Vasc Biol 25 : 1311-1320, 2005.

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