Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome. - Priestman, D; Neville, D; Reinkensmeier, G; Simpson, M; Proukakis, C; Patton, M; Dwek, R; Butters, T; Platt, F; Crosby, A (GLYCOBIOLOGY, 2004)