Mutation of the melastatin-related cation channel, TRPM3, underlies inherited cataract and glaucoma.
Inherited forms of cataract are a clinically important and genetically heterogeneous cause of visual impairment that usually present at an early age with or without systemic and/or other ocular abnormalities. Here we have identified a new locus for inherited cataract and high-tension glaucoma with v...
Збережено в:
| Автори: | , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Public Library of Science (PLoS)
2014-01-01
|
| Серія: | PLoS ONE |
| Онлайн доступ: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25090642/?tool=EBI |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|