Human Genome Epidemiology Literature Finder
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Query Trace: Epilepsy and TF[original query] |
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A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation. Journal of neurology 2015 Jan 262 (1): 154-64. Barone Rita, Carrozzi M, Parini R, Battini R, Martinelli D, Elia M, Spada M, Lilliu F, Ciana G, Burlina A, Leuzzi V, Leoni M, Sturiale L, Matthijs G, Jaeken J, Di Rocco M, Garozzo D, Fiumara |
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- Page last updated:Apr 22, 2024
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