Literature DB >> 1979681

Three RFLPs at the 3' end of the cystatin C gene, the disease gene in hereditary cystatin C amyloid angiopathy (HCCAA) in Iceland.

A Palsdottir1, S Jonsdottir, M Abrahamson, A Grubb, O Jensson.   

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Year:  1990        PMID： 1979681      PMCID： PMC332913          DOI： 10.1093/nar/18.24.7471-a

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  4 in total

1.  Mutation in cystatin C gene causes hereditary brain haemorrhage.

Authors:  A Palsdottir; M Abrahamson; L Thorsteinsson; A Arnason; I Olafsson; A Grubb; O Jensson
Journal:  Lancet       Date:  1988-09-10       Impact factor: 79.321

2.  Structure and expression of the human cystatin C gene.

Authors:  M Abrahamson; I Olafsson; A Palsdottir; M Ulvsbäck; A Lundwall; O Jensson; A Grubb
Journal:  Biochem J       Date:  1990-06-01       Impact factor: 3.857

3.  Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin C.

Authors:  M Abrahamson; A Grubb; I Olafsson; A Lundwall
Journal:  FEBS Lett       Date:  1987-06-01       Impact factor: 4.124

4.  The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20.

Authors:  M Abrahamson; M Q Islam; J Szpirer; C Szpirer; G Levan
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132
  4 in total
  1 in total

1.  A sequence variation in the human cystatin D gene resulting in an amino acid (Cys/Arg) polymorphism at the protein level.

Authors:  M Balbín; J P Freije; M Abrahamson; G Velasco; A Grubb; C López-Otín
Journal:  Hum Genet       Date:  1993-02       Impact factor: 4.132
  1 in total

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