Correction

Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy (vol 8, 14454, 2017)

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms16007

Keywords

-

Funding

  1. NHLBI NIH HHS [R01 HL122332] Funding Source: Medline
  2. NIAMS NIH HHS [R01 AR044533] Funding Source: Medline
  3. NICHD NIH HHS [U54 HD083091] Funding Source: Medline

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