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X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1).
Senderek, J.; Hermanns, B.; Bergmann, C. et al.
1999 • In Journal of the Neurological Sciences, 167 (2), p. 90-101

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X-linked dominant Charcot-Marie-Tooth neuropathy, clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1)..pdf

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