Domain specific mutations in dyskerin disrupt 3′ end processing of scaRNA13
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DOI: 10.1093/nar/gkac706
Abstract: Abstract 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,… read more here.
Keywords: scarna13; end; domain specific; domain ... See more keywords