MUTATION IN CYSTATIN C GENE CAUSES HEREDITARY BRAIN HAEMORRHAGE
- 10 September 1988
- journal article
- research article
- Published by Elsevier
- Vol. 332 (8611) , 603-604
- https://doi.org/10.1016/s0140-6736(88)90641-1
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin CPublished by Wiley ,2001
- Hereditary cystatin C (γ-trace) amyloid angiopathy of the CNS causing cerebral hemorrhageActa Neurologica Scandinavica, 1987
- Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosis.Stroke, 1987
- Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C).Proceedings of the National Academy of Sciences, 1986
- Gene organization and recombinational hotspots in the murine major histocompatibility complexCell, 1986
- Abnormal Metabolism of γ-Trace Alkaline MicroproteinNew England Journal of Medicine, 1984
- The place of human γ-trace (cystatin C) amongst the cysteine proteinase inhibitorsBiochemical and Biophysical Research Communications, 1984
- Correlation between a DNA restriction fragment length polymorphism and C4A6 proteinNature, 1983
- Human gamma-trace, a basic microprotein: amino acid sequence and presence in the adenohypophysis.Proceedings of the National Academy of Sciences, 1982
- Polymorphic DNA region adjacent to the 5' end of the human insulin gene.Proceedings of the National Academy of Sciences, 1981