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High-Throughput Analysis of Retinal Cis-Regulatory Networks by Massively Parallel Reporter Assays
Inherited retinal degenerations are diverse and debilitating blinding diseases. Genetic tests and exome sequencing have identified mutations in many protein-coding genes associated with such diseases, but causal sequence variants remain to be found in many retinopathy cases. Since 99% of our genome...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Adv Exp Med Biol |
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| Κύριοι συγγραφείς: | , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7001795/ https://ncbi.nlm.nih.gov/pubmed/31884638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-030-27378-1_59 |
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