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Domain specific mutations in dyskerin disrupt 3′ end processing of scaRNA13
Mutations in DKC1 (encoding dyskerin) cause telomere diseases including dyskeratosis congenita (DC) by decreasing steady-state levels of TERC, the non-coding RNA component of telomerase. How DKC1 mutations variably impact numerous other snoRNAs remains unclear, which is a barrier to understanding di...
Autores principales: | Nagpal, Neha, Tai, Albert K, Nandakumar, Jayakrishnan, Agarwal, Suneet |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458449/ https://www.ncbi.nlm.nih.gov/pubmed/36018809 http://dx.doi.org/10.1093/nar/gkac706 |
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