The history of research on facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary neuromuscular disease which is divided into FSHD1 and FSHD2. After years of research, FSHD has established complete molecular diagnostic methods, in which Southern blotting is commonly applied in the diagnosis of FSHD1, and molecul...
| 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/1950 |