Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination (Q55670897)

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article by L E Warner et al published September 1996 in Neuron
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Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
article by L E Warner et al published September 1996 in Neuron

    Statements

    Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination (English)
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    L E Warner
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    M J Hilz
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    S H Appel
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    J M Killian
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    E H Kolodry
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    G Karpati
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    S Carpenter
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    G V Watters
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    C Wheeler
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    D Witt
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    A Bodell
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    E Nelis
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    J R Lupski
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    September 1996
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    17
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    3
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    451-60
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