(Q28118945)
Statements
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De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III) (English)
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K. Hayasaka
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M. Himoro
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Y. Sawaishi
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K. Nanao
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T. Takahashi
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G. Takada
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G. A. Nicholson
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R. A. Ouvrier
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N. Tachi
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