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Two novel mutations in the bestrophin-1 gene and associated clinical observations in patients with best vitelliform macular dystrophy
The purpose of the current study was to investigate the 11 bestrophin-1 (BEST1) exons in patients with best vitelliform macular dystrophy (BVMD), and to characterize the associated clinical features. Complete ophthalmic examinations were conducted on two families, and two family members were diagnos...
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| Publicat a: | Mol Med Rep |
|---|---|
| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4464449/ https://ncbi.nlm.nih.gov/pubmed/25936525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2015.3711 |
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