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...
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| Udgivet i: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
National Academy of Sciences
1989
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| Fag: | |
| Online adgang: | 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 |
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