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Gene Therapy in the Retinal Degeneration Slow Model of Retinitis Pigmentosa

Human blinding disorders are often initiated by hereditary mutations that insult rod and/or cone photoreceptors and cause subsequent cellular death. Generally, the disease phenotype can be predicted from the specific mutation as many photoreceptor genes are specific to rods or cones; however certain...

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Hlavní autoři: Cai, Xue, Conley, Shannon M., Naash, Muna I.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2010
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3161507/
https://ncbi.nlm.nih.gov/pubmed/20238065
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4419-1399-9_70
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