Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence
- 1 March 2001
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 185 (1) , 31-37
- https://doi.org/10.1016/s0022-510x(01)00454-3
Abstract
No abstract availableKeywords
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