Recurrent episodes of spontaneous subconjunctival hemorrhage in patients with factor XIII Val34Leu mutation
- 1 December 2002
- journal article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 134 (6) , 927-929
- https://doi.org/10.1016/s0002-9394(02)01812-3
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- A common mutation in the gene for coagulation factor XIII‐A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseasesAmerican Journal of Hematology, 2001
- Blood Coagulation Factor XIII: Structure and FunctionThrombosis Research, 1999
- Genotype/Phenotype Correlations for Coagulation Factor XIII: Specific Normal Polymorphisms Are Associated With High or Low Factor XIII Specific ActivityBlood, 1999
- Association of a Common Polymorphism in the Factor XIII Gene With Venous ThrombosisBlood, 1999
- Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levelsBlood, 1994