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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...

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Bibliografski detalji
Izdano u:J Clin Invest
Glavni autori: Mason, Philip J., Bessler, Monica
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 2015
Teme:
Online pristup: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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