Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy
Main Authors: | , , , , , , , , , |
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Format: | Conference item |
Published: |
2005
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_version_ | 1797098384785408000 |
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author | Priestman, D Neville, D Reinkensmeier, G Simpson, M Proukakis, C Patten, M Dwek, R Butters, T Platt, F Crosby, A |
author_facet | Priestman, D Neville, D Reinkensmeier, G Simpson, M Proukakis, C Patten, M Dwek, R Butters, T Platt, F Crosby, A |
author_sort | Priestman, D |
collection | OXFORD |
description | |
first_indexed | 2024-03-07T05:08:46Z |
format | Conference item |
id | oxford-uuid:dad61f9b-01cc-4e86-a4f9-eff57d794733 |
institution | University of Oxford |
last_indexed | 2024-03-07T05:08:46Z |
publishDate | 2005 |
record_format | dspace |
spelling | oxford-uuid:dad61f9b-01cc-4e86-a4f9-eff57d7947332022-03-27T09:06:03ZHuman GM3 synthase deficiency: A novel form of hereditary childhood epilepsyConference itemhttp://purl.org/coar/resource_type/c_5794uuid:dad61f9b-01cc-4e86-a4f9-eff57d794733Symplectic Elements at Oxford2005Priestman, DNeville, DReinkensmeier, GSimpson, MProukakis, CPatten, MDwek, RButters, TPlatt, FCrosby, A |
spellingShingle | Priestman, D Neville, D Reinkensmeier, G Simpson, M Proukakis, C Patten, M Dwek, R Butters, T Platt, F Crosby, A Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title | Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title_full | Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title_fullStr | Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title_full_unstemmed | Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title_short | Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy |
title_sort | human gm3 synthase deficiency a novel form of hereditary childhood epilepsy |
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