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Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3‐like macular dystrophy
Stargardt disease‐3 (STGD3) is an autosomal dominant juvenile‐onset macular dystrophy characterized by progressive decreasing visual acuity, bilateral atrophic changes in the macula and absence of characteristic dark choroids. We identified a STGD3‐like macular dystrophy pedigree by clinical examina...
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| Publié dans: | J Cell Mol Med |
|---|---|
| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Blackwell Publishing Ltd
2007
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6740257/ https://ncbi.nlm.nih.gov/pubmed/16364203 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2005.tb00392.x |
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