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	Commenti a: Sarepta Therapeutics annuncia un programma per sottomettere una richiesta per un nuovo farmaco – New Drug application (NDA) – ai fini di un’approvazione accelerata di golodirsen (SRP-4053) nei pazienti con la distrofia muscolare di Duchenne (DMD) trattabili con l’exon skipping 53.	</title>
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	<description>Insieme per fermare la Duchenne e la Becker</description>
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