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Neurology|June 17, 1999

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotypeV Timmerman, P De Jonghe, C Ceuterick, et al.

Neuron|September 1, 1996

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.

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Showing results (11-20 of 12) with videos related to

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Neurology|June 17, 1999

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotypeV Timmerman, P De Jonghe, C Ceuterick, et al.

Neuron|September 1, 1996

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.

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