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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Dades bibliogràfiques
Publicat a:Hum Mol Genet
Autors principals: Farrar, G. Jane, Carrigan, Matthew, Dockery, Adrian, Millington-Ward, Sophia, Palfi, Arpad, Chadderton, Naomi, Humphries, Marian, Kiang, Anna Sophia, Kenna, Paul F., Humphries, Pete
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2017
Matèries:
Invited Reviews
Accés en línia: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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