تحميل...
Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations
To assess the progression of Stargardt (STGD) disease over nine years in two branches of a large consanguineous Tunisian family. Initially, different phenotypes were observed with clinical intra- and interfamilial variations. At presentation, four different retinal phenotypes were observed. In pheno...
محفوظ في:
| الحاوية / القاعدة: | J Ophthalmol |
|---|---|
| المؤلفون الرئيسيون: | , , , , , , |
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Hindawi
2018
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| الموضوعات: | |
| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5875050/ https://ncbi.nlm.nih.gov/pubmed/29736279 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/1030184 |
| الوسوم: |
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