Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease
<p>Abstract</p> <p>Background</p> <p>X-linked Charcot-Marie Tooth (CMT) is caused by mutations in the connexin32 gene that encodes a polypeptide which is arranged in hexameric array and form gap junctions.</p> <p>Methods</p> <p>We describe two no...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2007-07-01
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| Series: | BMC Neurology |
| Online Access: | http://www.biomedcentral.com/1471-2377/7/19 |