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Human GM3 synthase deficiency:...
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Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy
Bibliographic Details
Main Authors:
Priestman, D
,
Neville, D
,
Reinkensmeier, G
,
Simpson, M
,
Proukakis, C
,
Patten, M
,
Dwek, R
,
Butters, T
,
Platt, F
,
Crosby, A
Format:
Conference item
Published:
2005
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