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Evolutionary Dynamics of Abundant Stop Codon Readthrough.

Molecular Biology and Evolution, 2016
Manolis Kellis   +2 more
exaly  

The aminoglycoside geneticin permits translational readthrough of the CTNS W138X nonsense mutation in fibroblasts from patients with nephropathic cystinosis

Pediatric Nephrology, 2018
Paul Goodyer, Robin Loesch
exaly  
medicine
nonsense mutation
genetics
premature termination codon
readthrough
nonsense mutations
genetic diseases
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