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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| Опубликовано в:: | Proc Natl Acad Sci U S A |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
National Academy of Sciences
1989
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| Предметы: | |
| Online-ссылка: | 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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