User talk:Melrosejackson/sandbox

Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy, affecting around 1 in 3,600 males, which results in muscle degeneration and premature death.[1] The disorder is caused by a mutation in the dystrophin gene, located on the human X chromosome, which codes for the protein dystrophin. Dystrophin is an important structural component within muscle tissue that provides structural stability to the dystroglycan complex (DGC) of the cell membrane. While both sexes can carry the mutation, females rarely exhibit signs of the disease.

Rewrite and review version April 29, 2015:Duchenne muscular dystrophy (DMD) is a recessive X-link form of muscular dystrophy,affecting about 1 in 3,600 males, which results in muscle deterioration and premature death.[1] The disorder is caused by a mutation in the dystrophin gene, located on the human X chromosome, which codes for the protein dystrophin. Dystrophin is an important structural component within the muscle tissue that provides structural stability to the dystroglycan complex(DGC) of the cell membrane. While both sexes carry the mutation, females rarely exhibit signs of the disease. — Preceding unsigned comment added by Melrosejackson (talk • contribs) 23:36, 29 April 2015 (UTC)

Thanks
Thanks for the superior work here. You've done well. Pindham (talk) 17:25, 27 May 2015 (UTC)