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CMT1X phenotypes represent loss of
GJB1
gene function
Neurology Shy et al. 68: 849
Data Supplement
One figure and one table; one PowerPoint and one Word document.
Files in this Data Supplement:
E1
- Figure; PowerPoint document.
E1
- E-Table 1: Connexin 32 mutations involved in study; Word document.
This Article
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