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Werner's Syndrome (WS) or adult-onset progeria is an autosomal recessive disorder of accelerated aging caused by mutations of the DNA RecQ helicase/exonuclease (WRN). WRN is an ATP-dependent helicase with 3′ to 5′ DNA exonuclease activity that re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22fd45f2ef4b400f91d2c928d9cb87a0
https://europepmc.org/articles/PMC3071901/
https://europepmc.org/articles/PMC3071901/
Publikováno v:
Hawaii Medical Journal; Mar2011, Vol. 70 Issue 3, p52-55, 4p
