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Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon.

Archive ouverte | Rederstorff, M. | CCSD

International audience. Premature termination of translation due to nonsense mutations is a frequent cause of inherited diseases. Therefore, many efforts were invested in the development of strategies or compounds t...

Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon

Archive ouverte | Rederstorff, M. | CCSD

International audience

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Archive ouverte | Stojkovic, T. | CCSD

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