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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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| Publicado no: | J Cell Mol Med |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2007
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| Assuntos: | |
| Acesso em linha: | 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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