Priestman, DA and Neville, DCA and Reinkensmeier, G and Simpson, MA and Proukakis, C and Patton, MA and Dwek, RA and Butters, TD and Platt, FM and Crosby, AH (2004) Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome. In: GLYCOBIOLOGY. (pp. 1179 - 1179). OXFORD UNIV PRESS INC
Full text not available from this repository.
| Type: | Proceedings paper |
|---|---|
| Title: | Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome. |
| Event: | Joint Meeting of the Society-for-Glycobiology/Japanese-Society-for-Carbohydrate-Research |
| Location: | Honolulu, HI |
| Dates: | 2004-11-17 - 2004-11-20 |
| UCL classification: | UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Clinical Neuroscience |
Archive Staff Only: edit this record