No abstract available
MeSH terms
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Brain / pathology
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Central Nervous System Diseases / genetics
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Charcot-Marie-Tooth Disease / diagnosis*
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Charcot-Marie-Tooth Disease / genetics
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Child
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Connexins / genetics
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Demyelinating Diseases / diagnosis*
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Encephalomyelitis / diagnosis*
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Gap Junction beta-1 Protein
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Humans
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Magnetic Resonance Imaging
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Male
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Mutation
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Phenotype