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NEW EMBO MEMBER’S REVIEW: On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention

Retinitis pigmentosa (RP), the group of hereditary conditions involving death of retinal photoreceptors, represents the most prevalent cause of visual handicap among working populations in developed countries. Here we provide an overview of the molecular pathologies associated with such disorders, f...

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Detalhes bibliográficos
Main Authors: Farrar, G.Jane, Kenna, Paul F., Humphries, Peter
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2002
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC125887/
https://ncbi.nlm.nih.gov/pubmed/11867514
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/21.5.857
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