Genetic Polymorphisms of Transcription Factor NRF2 and of its Host Gene Sulfiredoxin (SRXN1) are Associated with Cerebrovascular Disease in a Finnish Cohort, the TAMRISK Study

Tarja Kunnas, Kirsi Määttä, Seppo T. Nikkari

Research output: Contribution to journalArticleScientificpeer-review

19 Citations (Scopus)
Original languageEnglish
Pages (from-to)325-329
JournalInternational Journal of Medical Sciences
Volume13
Issue number5
DOIs
Publication statusPublished - 2016
Publication typeA1 Journal article-refereed

Keywords

  • Cerebrovascular Disorders
  • Genetic Predisposition to Disease/genetics
  • NF-E2-Related Factor 2/genetics
  • Oxidoreductases Acting on Sulfur Group Donors/genetics

Publication forum classification

  • Publication forum level 1

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