Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome.

Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome.

Detalhes bibliográficos
Main Authors: Priestman, D, Neville, D, Reinkensmeier, G, Simpson, M, Proukakis, C, Patton, M, Dwek, R, Butters, T, Platt, F, Crosby, A
Formato: Conference item
Publicado em: 2004

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