Progress in treatment of Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease (CMT) comprises a group of monogenic inherited peripheral neuropathies with highly clinical and genetic heterogeneity, more than 80 causative genes have been cloned at present. Usually starts in childhood or juvinile period, the main clinical manifestations include progre...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Tianjin Huanhu Hospital
2017-08-01
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Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
Subjects: | |
Online Access: | http://www.cjcnn.org/index.php/cjcnn/article/view/1640 |