MUT-7 Provides Molecular Insight into the Werner Syndrome Exonuclease

Werner syndrome (WS) is a rare recessive genetic disease characterized by premature aging. Individuals with this disorder develop normally during childhood, but their physiological conditions exacerbate the aging process in late adolescence. WS is caused by mutation of the human WS gene (WRN), which...

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Detalles Bibliográficos
Autores principales: Hsu, Tsung-Yuan, Hsu, Ling-Nung, Chen, Shih-Yu, Juang, Bi-Tzen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700014/
https://www.ncbi.nlm.nih.gov/pubmed/34943966
http://dx.doi.org/10.3390/cells10123457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700014/
https://www.ncbi.nlm.nih.gov/pubmed/34943966
http://dx.doi.org/10.3390/cells10123457

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