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C1q enhances cone photoreceptor survival in a mouse model of autosomal recessive retinitis pigmentosa

Retinitis pigmentosa (RP) is a degenerative retinal disease involving progressive loss of rod and cone photoreceptor function. It represents the most common form of registered blindness among the working aged populations of developed countries. Given the immense genetic heterogeneity associated with...

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Detalhes bibliográficos
Main Authors: Humphries, Marian M, Kenna, Paul F, Campbell, Matthew, Tam, Lawrence C S, Nguyen, Anh T H, Farrar, G Jane, Botto, Marina, Kiang, Anna Sophia, Humphries, Peter
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3234518/
https://ncbi.nlm.nih.gov/pubmed/21863053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.151
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