Mutator phenotype of Werner syndrome is characterized by extensive deletions.
Werner syndrome (WS) is a rare autosomal-recessive disorder characterized by the premature appearance of features of normal aging in young adults. The extensive phenotypic overlap between WS and normal aging suggests they may also share pathogenetic mechanisms. We reported previously that somatic ce...
Guardat en:
| Publicat a: | Proc Natl Acad Sci U S A |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1989
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC297737/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2762303/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.15.5893 |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|