Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A von Chapon, F, Diraison, P, Lechevalier, B, Chazot, G, Viader, F, Bonnebouche, C, Vandenberghe, A, Timmerman, V, Van Broeckhoven, C

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Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B von Latour, Philippe, Blanquet, Françoise, Nelis, Eva, Bonnebouche, Christine, Chapon, Fraņoise, Diraison, Philippe, Ollagnon, Elisabeth, Dautigny, André, Pham-Dinh, Danielle, Chazot, Guy, Boucherat, Michel, Van Broeckhoven, Christine, Vandenberghe, Antoon

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Charcot-Marie-Tooth type 1B neuropathy: A mutation at the single glycosylation site in the major peripheral myelin glycoprotein P0 von Blanquet-Grossard, Françoise, Pham-Dinh, Danielle, Dautigny, André, Latour, Philippe, Bonnebouche, Christine, Diraison, Philippe, Chapon, Françoise, Chazot, Guy, Vandenberghe, Antoon

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Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po von Blanquet-Grossard, F, Pham-Dinh, D, Dautigny, A, Latour, P, Bonnebouche, C, Diraison, P, Chapon, F, Chazot, G, Vandenberghe, A

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Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A von Chapon, F, Diraison, P, Lechevalier, B, Chazot, G, Viader, F, Bonnebouche, C, Vandenberghe, A, Timmerman, V, Van Broeckhoven, C

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