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mRNA deadenylation and telomere disease
Dyskeratosis congenita (DC) is an inherited BM failure disorder that is associated with mutations in genes involved with telomere function and maintenance; however, the genetic cause of many instances of DC remains uncharacterized. In this issue of the JCI, Tummala and colleagues identify mutations...
Sparad:
| I publikationen: | J Clin Invest |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Society for Clinical Investigation
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4463216/ https://ncbi.nlm.nih.gov/pubmed/25893598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI81506 |
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