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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Detalles Bibliográficos
Autores principales: Farrar, G. Jane, Carrigan, Matthew, Dockery, Adrian, Millington-Ward, Sophia, Palfi, Arpad, Chadderton, Naomi, Humphries, Marian, Kiang, Anna Sophia, Kenna, Paul F., Humphries, Pete
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Invited Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886474/
https://www.ncbi.nlm.nih.gov/pubmed/28510639
http://dx.doi.org/10.1093/hmg/ddx185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886474/
https://www.ncbi.nlm.nih.gov/pubmed/28510639
http://dx.doi.org/10.1093/hmg/ddx185

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