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Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy

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APA Style

Priestman, D., Neville, D., Reinkensmeier, G., Simpson, M., Proukakis, C., Patten, M., Dwek, R., Butters, T., Platt, F., & Crosby, A. (2005). Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy. GLYCOBIOLOGY, 15(11), 1192–1192.

MLA Style

Priestman, D., et al. “Human GM3 Synthase Deficiency: A Novel Form of Hereditary Childhood Epilepsy.” GLYCOBIOLOGY, vol. 15, no. 11, 2005, pp. 1192–92.

Chicago Style

Priestman, D, D Neville, G Reinkensmeier, M Simpson, C Proukakis, M Patten, R Dwek, T Butters, F Platt, and A Crosby. 2005. “Human GM3 Synthase Deficiency: A Novel Form of Hereditary Childhood Epilepsy.” In GLYCOBIOLOGY, 15:1192–92.
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+ Priestman, D More by this author

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+ Neville, D More by this author

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+ Reinkensmeier, G More by this author

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+ Simpson, M More by this author

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+ Proukakis, C More by this author

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Host title:: GLYCOBIOLOGY
Volume:: 15
Issue:: 11
Pages:: 1192-1192
Publication date:: 2005-11-01
ISSN:: 0959-6658

Pubs id:: pubs:185303
UUID:: uuid:dad61f9b-01cc-4e86-a4f9-eff57d794733
Local pid:: pubs:185303
Source identifiers:: 185303
Deposit date:: 2012-12-19

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Copyright date:: 2005

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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