Lataa...
Identification of cis-regulatory sequence variations in individual genome sequences
Functional contributions of cis-regulatory sequence variations to human genetic disease are numerous. For instance, disrupting variations in a HNF4A transcription factor binding site upstream of the Factor IX gene contributes causally to hemophilia B Leyden. Although clinical genome sequence analysi...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3239227/ https://ncbi.nlm.nih.gov/pubmed/21989199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm281 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|