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Muscular dystrophy research papers

Click on image for details. Muscular dystrophy is a genetic disorder leading to progressive weakness of muscles caused due to dysfunction in or lack of protein in muscle cells. The prevalence of muscular dystrophy has been observed globally and is becoming a critical area of study for better health services. The purpose of the study is to analyze the research strength of muscular dystrophy using bibliographic literature.
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Duchenne Muscular Dystrophy Research Paper

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Duchenne's Muscular Dystrophy Research Paper - Words | Cram

This has become a reality for many parents as they find out that their child has a form of muscular dystrophy. This particular type of muscular dystrophy is referred to as Duchenne Muscular Dystrophy, which is a genetically inherited disorder that is the most common and severe of all muscular dystrophies. It is found in 1 of every 3, males and is characterized by progressive muscle wasting. It is caused by the lack of dystrophin, which is a protein. Duchenne's muscular dystrophy, also known as psuedohypertrophic muscular dystrophy, is a typical sex-linked disorder in which the muscles degenerate throughout a person's life. It literally means "faulty nutrition of the muscles.
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Muscular Dystrophy Papers

This has become a reality for many parents as they find out that their child has a form of muscular. This particular type of muscular dystrophy is referred to as Duchenne Muscular Dystrophy, which is a genetically inherited disorder that is the most common and severe of all muscular dystrophies. It is found in 1 of every 3, males and is characterized by progressive muscle wasting. It is caused by the lack of dystrophin, which is a protein found in the cell membrane of muscles.
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Please join StudyMode to read the full document. The muscles of the heart and some other involuntary muscles are also affected in some forms of muscular dystrophy , and a few forms involve other organs as well. That landmark finding revealed one of the first genes ever connected to an inherited disease. We constantly work to improve the care we are able to give our patients. We conduct numerous clinical studies on neuromuscular diseases, and we are one of five sites in the United States funded by the Muscular Dystrophy Association to conduct multi-center clinical studies.
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