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Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes
De novo variants (DNVs) are critical to the treatment of neurodevelopmental disorders (NDDs). However, effectively identifying candidate genes in small cohorts is challenging in most NDDs because of high genetic heterogeneity. We hypothesised that integrating DNVs from multiple NDDs with genetic sim...
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| Vydáno v: | Life (Basel) |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8001830/ https://ncbi.nlm.nih.gov/pubmed/33809095 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/life11030233 |
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