Werner Syndrome Protein and DNA Replication

Werner Syndrome (WS) is an autosomal recessive disorder characterized by the premature development of aging features. Individuals with WS also have a greater predisposition to rare cancers that are mesenchymal in origin. Werner Syndrome Protein (WRN), the protein mutated in WS, is unique among RecQ...

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Detalles Bibliográficos
Autores principales: Mukherjee, Shibani, Sinha, Debapriya, Bhattacharya, Souparno, Srinivasan, Kalayarasan, Abdisalaam, Salim, Asaithamby, Aroumougame
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274846/
https://www.ncbi.nlm.nih.gov/pubmed/30400178
http://dx.doi.org/10.3390/ijms19113442

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274846/
https://www.ncbi.nlm.nih.gov/pubmed/30400178
http://dx.doi.org/10.3390/ijms19113442

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