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Duchenne muscular dystrophy: an updated review of common available therapies.

Arash SalmaninejadSaeed Farajzadeh ValilouHadi BayatNader EbadiAbdolreza DaraeiMeysam YousefiAbolfazl NesaeiMajid Mojarrad
Published in: The International journal of neuroscience (2018)
This review provides an update on the recent gene therapies for DMD that aim to compensate for dystrophin deficiency and the related clinical trials.
Keyphrases
  • duchenne muscular dystrophy
  • clinical trial
  • muscular dystrophy
  • genome wide
  • randomized controlled trial
  • gene expression
  • study protocol
  • dna methylation
  • genome wide identification