Additionally, intra‐amniotic injection of rAAV9‐micro‐dystrophin in a beagle X‐linked model of DMD (CXMDJ) demonstrated improvements in respiratory function, as shown by whole‐body plethysmography (Table 5; Hayashita‐Kinoh et al., 2015). The gene discussed is DMD; the disease is Duchenne muscular dystrophy.