Загрузка...
Structure of the human MLH1 N-terminus: implications for predisposition to Lynch syndrome
Mismatch repair prevents the accumulation of erroneous insertions/deletions and non-Watson–Crick base pairs in the genome. Pathogenic mutations in the MLH1 gene are associated with a predisposition to Lynch and Turcot’s syndromes. Although genetic testing for these mutations is available, robust cla...
Сохранить в:
| Опубликовано в: : | Acta Crystallogr F Struct Biol Commun |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
International Union of Crystallography
2015
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4528928/ https://ncbi.nlm.nih.gov/pubmed/26249686 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1107/S2053230X15010183 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|