Related content

Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A

By  

Molecular Syndromology, Vol. 7, Iss. 4, 2016-07 ,pp. : 182-188

Karger

Access to resources Recommend Favorite

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

By Martin Melinda S.   Tang Bin   Papale Ligia A.   Yu Frank H.   Catterall William A.   Escayg Andrew  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2892-2899

Oxford University Press

Access to resources Recommend Favorite

Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins

By Spencer Corinne M.   Serysheva Ekaterina   Yuva-Paylor Lisa A.   Oostra Ben A.   Nelson David L.   Paylor Richard  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 1984-1994

Oxford University Press

Access to resources Recommend Favorite

Genetic Animal Models for Absence Epilepsy: A Review of the WAG/Rij Strain of Rats

By Coenen A.M.L.  

Behavior Genetics, Vol. 33, Iss. 6, 2003-11 ,pp. : 635-655

Springer Publishing Company

Access to resources Recommend Favorite

Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of Tuberous Sclerosis Complex

By Zeng Ling-Hui   Rensing Nicholas R.   Zhang Bo   Gutmann David H.   Gambello Michael J.   Wong Michael  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 445-454

Oxford University Press

Access to resources Recommend Favorite