MeSH Browser

MeSH Supplementary: Wrn protein, mouse
Unique ID: C499253
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C499253
Entry Term(s): Werner syndrome protein, mouse
Registry Numbers: EC 3.6.4.12
Previous Indexing: *DNA HELICASES (2005-2006); *RECQ HELICASES (2006-2016)
Heading Mapped to: *Werner Syndrome Helicase
Frequency: 39
Note: the protein responsible for Werner's syndrome homolog in mice, an inherited disease with clinical symptoms resembling premature aging; RefSeq NM_011721
Source: Cancer Genet Cytogenet 2005 Jan 15;156(2):134-43
Indexing Information: Werner Syndrome
Date of Entry: 2005/04/11
Revision Date: 2016/04/18

Wrn protein, mouse MeSH Supplementary Concept Data 2025