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Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

✍ Scribed by Simpson, Michael A; Cross, Harold; Proukakis, Christos; Priestman, David A; Neville, David C A; Reinkensmeier, Gabriele; Wang, Heng; Wiznitzer, Max; Gurtz, Kay; Verganelaki, Argyro


Book ID
109919073
Publisher
Nature Publishing Group
Year
2004
Tongue
English
Weight
392 KB
Volume
36
Category
Article
ISSN
1061-4036

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