Advance and cogitation of gene therapy for Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is the common hereditary muscular disease caused by the deficiency of cytoskeletal protein dystrophin on the sarcolemma. It is characterized by progessive muscle weakness and atrophy and dying of heart or respiratory failure. Currently the gene therapy strategies of...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Tianjin Huanhu Hospital
2019-05-01
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| Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Subjects: | |
| Online Access: | http://cjcnn.org/index.php/cjcnn/article/view/1951 |