Chargement en cours...
Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options
Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy and is associated with disease-causing sequence variants in the gene ABCA4. Significant advances have been made over the last 10 years in our understanding of both the clinical and molecular features of STGD1, an...
Enregistré dans:
| Publié dans: | Br J Ophthalmol |
|---|---|
| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BMJ Publishing Group
2017
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5256119/ https://ncbi.nlm.nih.gov/pubmed/27491360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjophthalmol-2016-308823 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|