טוען...
A model for familial exudative vitreoretinopathy caused by LPR5 mutations
We have identified a mouse recessive mutation that leads to attenuated and hyperpermeable retinal vessels, recapitulating some pathological features of familial exudative vitreoretinopathy (FEVR) in human patients. DNA sequencing reveals a single nucleotide insertion in the gene encoding the low-den...
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| Main Authors: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2008
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2902293/ https://ncbi.nlm.nih.gov/pubmed/18263894 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn047 |
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