Загрузка...
Is HSPG2 a modifier gene for Marfan syndrome?
Marfan syndrome (MFS) is a connective tissue disease caused by variants in the FBN1 gene. Nevertheless, other genes influence the manifestations of the disease, characterized by high clinical variability even within families. We mapped modifier loci for cardiovascular and skeletal manifestations in...
Сохранить в:
| Опубликовано в: : | Eur J Hum Genet |
|---|---|
| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Springer International Publishing
2020
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7608216/ https://ncbi.nlm.nih.gov/pubmed/32514132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-0666-0 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|