Article
Werner syndrome: entering the helicase era.
BioEssays : news and reviews in molecular, cellular and developmental biology - 1 Dec 1996
Epstein C J, Motulsky A G
Abstract excerpt
Werner syndrome is a rare autosomal recessive disorder that mimics some of the characteristics of aging. The gene for this disorder has recently been identified as a helicase of the recQ subclass. Other phenotypically distinctive disorders caused by different helicase mutations include Bloom syndrome, Cockayne syndrome, xeroderma pigmentosum and trichothiodystrophy. Possible mechanisms by which helicases might...
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