Natural history of Duchenne muscular dystrophy
<p>Duchenne muscular dystrophy (DMD) is X-linked recessive hereditary disease. <em>DMD</em> gene mutations result in dystrophin deficiency, which causes not only muscle movement disorders but also scoliosis, cognitive dysfunction, urinary tract diseases, respiratory diseases and heart diseases. Most...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Tianjin Huanhu Hospital
2015-05-01
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| Col·lecció: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Matèries: | |
| Accés en línia: | http://www.cjcnn.org/index.php/cjcnn/article/view/1189 |
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