G.P.168

• Published in: Neuromuscular disorders : NMD Vol. 24; no. 9; p. 856
• Main Authors: Preuße, C, Schara, U, Goebel, H.H, Zerbe, N, Hufnagl, P, Heppner, F.L, von Moers, A, Stenzel, W
• Format: Journal Article
• Language: English
• Published: 01.10.2014
• Subjects: Neurology

As the most frequent genetic muscle disease worldwide, Duchenne Muscular Dystrophy affects ∼1:5 000 male births. Caused by a defective DMD gene, the dystrophin protein expression is severely hampered and the protein is only partially functional or completely dysfunctional. The constant breakdown of...