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Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome.

Publication status:: Published

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APA Style

Priestman, D., Neville, D., Reinkensmeier, G., Simpson, M., Proukakis, C., Patton, M., Dwek, R., Butters, T., Platt, F., & Crosby, A. (2004). Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome. GLYCOBIOLOGY, 14(11), 1179–1179.

MLA Style

Priestman, D., et al. “Human GM3 Synthase Deficiency: Autosomal Recessive Infantile Onset Symptomatic Epilepsy Syndrome.” GLYCOBIOLOGY, vol. 14, no. 11, 2004, pp. 1179–79.

Chicago Style

Priestman, D, D Neville, G Reinkensmeier, M Simpson, C Proukakis, M Patton, R Dwek, T Butters, F Platt, and A Crosby. 2004. “Human GM3 Synthase Deficiency: Autosomal Recessive Infantile Onset Symptomatic Epilepsy Syndrome.” In GLYCOBIOLOGY, 14:1179–79.
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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:: 14
Issue:: 11
Pages:: 1179-1179
Publication date:: 2004-11-01
ISSN:: 0959-6658

Pubs id:: pubs:185148
UUID:: uuid:256100c7-5698-43ac-a8ff-7071f8f708e1
Local pid:: pubs:185148
Source identifiers:: 185148
Deposit date:: 2012-12-19

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Copyright date:: 2004

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

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