Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype.

Published in:

Human Molecular Genetics, 2012, v. 21, n. 4, p. 811, doi. 10.1093/hmg/ddr512

By:

• Pierson, Christopher R.;
• Dulin-Smith, Ashley N.;
• Durban, Ashley N.;
• Marshall, Morgan L.;
• Marshall, Jordan T.;
• Snyder, Andrew D.;
• Naiyer, Nada;
• Gladman, Jordan T.;
• Chandler, Dawn S.;
• Lawlor, Michael W.;
• Buj-Bello, Anna;
• Dowling, James J.;
• Beggs, Alan H.

Publication type:

Article