Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.

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Published in Nat Genet on October 24, 2004

Authors

Michael A Simpson1, Harold Cross, Christos Proukakis, David A Priestman, David C A Neville, Gabriele Reinkensmeier, Heng Wang, Max Wiznitzer, Kay Gurtz, Argyro Verganelaki, Anna Pryde, Michael A Patton, Raymond A Dwek, Terry D Butters, Frances M Platt, Andrew H Crosby

Author Affiliations

1: Department of Medical Genetics, St. George's Hospital Medical School, University of London, Cranmer Terrace, London SW17 0RE, UK.

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