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EXONIC SINE INSERTION IN STK38L CAUSES CANINE EARLY RETINAL DEGENERATION (erd)
Fine mapping followed by candidate gene analysis of erd - a canine hereditary retinal degeneration characterized by aberrant photoreceptor development - established that the disease cosegregates with a SINE insertion in exon 4 of the canine STK38L/NDR2 gene. The mutation removes exon 4 from STK38L t...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2996878/ https://ncbi.nlm.nih.gov/pubmed/20887780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2010.09.003 |
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