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‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration
Inherited retinal degeneration (IRD), a leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. During the past decades, tremendous efforts have been made to explore the complex heterogeneity, and massive mutations have been identif...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4060621/ https://ncbi.nlm.nih.gov/pubmed/24939193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/bau047 |
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