Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion - Gouider, R; LeGuern, E; Gugenheim, M; Tardieu, S; Maisonobe, T; Leger, JM; Vallat, JM; Agid, Y; Bouche, P; Brice, A (Neurology, 1995)
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