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Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria

✍ Scribed by Kate M. Lawrence; Davide Mei; Mark R. Newton; Richard J. Leventer; Renzo Guerrini; Samuel F. Berkovic


Book ID
109112818
Publisher
Wiley (Blackwell Publishing)
Year
2010
Tongue
English
Weight
262 KB
Volume
51
Category
Article
ISSN
0013-9580

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