Загрузка...
A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family
PURPOSE: To identify the pathogenic gene mutation in a Chinese family with autosomal dominant congenital nuclear cataract. METHODS: After obtaining informed consent, detailed ophthalmic examinations were performed and genomic DNAs were obtained from eleven family members in a three-generation Chines...
Сохранить в:
| Главные авторы: | , , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Molecular Vision
2011
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3081795/ https://ncbi.nlm.nih.gov/pubmed/21527994 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|