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Toward an elucidation of the molecular genetics of inherited retinal degenerations
While individually classed as rare diseases, hereditary retinal degenerations (IRDs) are the major cause of registered visual handicap in the developed world. Given their hereditary nature, some degree of intergenic heterogeneity was expected, with genes segregating in autosomal dominant, recessive,...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886474/ https://ncbi.nlm.nih.gov/pubmed/28510639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx185 |
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