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De Novo SCN2A Mutations Cause Variable Phenotypes in Children with Epilepsy
De Novo SCN2A Mutations Cause Variable Phenotypes in Children with Epilepsy
2014
Markus Wolff
T. Bast
Tobias Loddenkemper
D. Jillella
Miriam Döcker
L. Wong-Kisiel
Rikke S. Møller
Sarah Weckhuysen
Berten Ceulemans
J. Klepper
F. Baumeister
C Finetti
G. Kurlemann
Hiltrud Muhle
Gerhard Kluger
Keywords:
Epilepsy
Phenotype
Diabetes mellitus
Medicine
Pathology
Bioinformatics
Correction
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