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What is the missing molecule in Duchenne muscular dystrophy?
The missing molecule in Duchenne muscular dystrophy is dystrophin, which is a protein that helps maintain the structure and function of muscle cells. In individuals with Duchenne muscular dystrophy, mutations in the DMD gene lead to a deficiency or absence of dystrophin protein.
What is FSHD?
Facio scapulo humerous dystrophy, a form of muscular dystrophy.
How does muscular dystrophy disrupt homeostasis?
The muscular Dystrophy do not maintain homeostasis.
Can you give a sentence for the word dystrophy?
The tests revealed that he was suffering from muscular dystrophy.
When was Muscular Dystrophy Association created?
Muscular Dystrophy Association was created in 1950.
How does muscular dystrophy progress?
Muscular dytrophy is not spread it is heriditary.
What is dystrophy?
Muscular dystrophy (MD) is a genetic disorder that weakens the muscles that help the body move.
The form of muscular dystrophy in which survival is rarely beyond the late twenties?
Duchenne's muscular dystrophy
What is the most common and most severe type of muscular dystrophy in children?
Duchenne Muscular Dystrophy
What are goals of rehabilitation for someone with muscular dystrophy?
what are the goals fo rehabilitation for someone with muscular dystrophy
When was Muscular Dystrophy Family Foundation created?
Muscular Dystrophy Family Foundation was created in 1958.
When was Muscular Dystrophy Campaign Trailblazers created?
Muscular Dystrophy Campaign Trailblazers was created in 2008.
