(Q35451458)
Statements
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Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene (English)
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Chapon F
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Latour P
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Diraison P
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Schaeffer S
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Vandenberghe A
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1 June 1999
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66
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6
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779-782
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Identifiers
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