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
Publicado en:Hum Mol Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2017
Assuntos:
Invited Reviews
Acceso en liña: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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