Clinical symptoms and molecular biology research in a family with oculopharyngeal muscular dystrophy
Objective To investigate the clinical symptoms and molecular biological characteristics in a family with oculopharyngeal muscular dystrophy (OPMD). Methods Clinical data of the family members were collected. Genomic DNA were isolated from peripheral blood of 6 family members including the probands f...
Збережено в:
| Автори: | , , , , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Tianjin Huanhu Hospital
2021-06-01
|
| Серія: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Предмети: | |
| Онлайн доступ: | http://www.cjcnn.org/index.php/cjcnn/article/view/2343 |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|