Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome.
Main Authors: | Priestman, D, Neville, D, Reinkensmeier, G, Simpson, M, Proukakis, C, Patton, M, Dwek, R, Butters, T, Platt, F, Crosby, A |
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Format: | Conference item |
Published: |
2004
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