Protein C Deficiency: A Database of Mutations
- 1 January 1993
- journal article
- research article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 69 (01) , 077-084
- https://doi.org/10.1055/s-0038-1651552
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequencesHuman Genetics, 1992
- Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosisHuman Genetics, 1992
- Treatment of Homozygous Protein C Deficiency and Neonatal Purpura Fulminans with a Purified Protein C ConcentrateNew England Journal of Medicine, 1991
- Late-onset homozygous protein C deficiencyThe Lancet, 1991
- A new hereditary abnormal protein C (protein C Yonago) with a dysfunctional Gla-domainThrombosis Research, 1991
- Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environmentHuman Genetics, 1991
- A single base-pair deletion in the protein C gene causing recurrent thromboembolismThrombosis Research, 1991
- A Thrombotic State Due to an Abnormal Protein CNew England Journal of Medicine, 1988
- Absence of Thrombosis in Subjects with Heterozygous Protein C DeficiencyNew England Journal of Medicine, 1987
- Homozygous Protein C Deficiency Manifested by Massive Venous Thrombosis in the NewbornNew England Journal of Medicine, 1984