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Infantile neuropathy with unstable myelin: study of the P0 protein
S Peudenier1, J F Deleuze, D Pham-Dinh
1Service de Neuropédiatrie, CHU de Bicêtre, Le Kremlin-Bicêtre, France.
Journal of Neurology
|May 1, 1993
Abstract:
An unusual form of hereditary motor and sensory neuropathy characterized by a prominent disruption of the myelin lamellae is reported. In addition to detailed morphological analysis, we investigated the protein P0, which is the major protein of peripheral myelin involved in adhesion. No major gene rearrangement and no differences in P0 protein expression were observed in the present case.