Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

Familial Adult Myoclonic Epilepsy

(2012) Lynette G. Sadleir   ARCHIVES OF NEUROLOGY

Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy

(2011) Antonietta Coppola et al.   EPILEPSIA

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree

(2011) Satsuki Mori et al.   JOURNAL OF HUMAN GENETICS

Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification

(2010) Pasquale Striano et al.   EPILEPSY & BEHAVIOR

Familial cortical myoclonic tremor with epilepsy: The third locus (FCMTE3) maps to 5p

(2010) C. Depienne et al.   NEUROLOGY

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

Multiple Molecular Interactions Determine the Clustering of Caspr2 and Kv1 Channels in Myelinated Axons

(2008) I. Horresh et al.   JOURNAL OF NEUROSCIENCE

Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes

(2008) Maria Savvaki et al.   MOLECULAR AND CELLULAR NEUROSCIENCE