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Werner Syndrome

1 Jan 2002

Abstract excerpt

Werner syndrome is a premature aging disease caused by the mutation in the WRN gene. The cloning and characterization of the WRN gene and its product allows investigators to study the disease and the human aging process at molecular level. This review summarizes the recent progresses on various aspects of the WRN research including functional analysis of the protein, interactive cloning, complexes formation,...

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Identifiers

PMID: 12488583
DOI: 10.1155/s1110724302201011

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