Mutations of DEPDC5 cause autosomal dominant focal epilepsies

Familial focal epilepsy with variable foci mapped to chromosome 22q12: Expansion of the phenotypic spectrum

(2012) Karl Martin Klein et al.   EPILEPSIA

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

(2012) Sarah E Heron et al.   NATURE GENETICS

A Conserved Coatomer-related Complex Containing Sec13 and Seh1 Dynamically Associates With the Vacuole inSaccharomyces cerevisiae

(2011) Svetlana Dokudovskaya et al.   MOLECULAR & CELLULAR PROTEOMICS

Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers

(2011) Daiki Miki et al.   NATURE GENETICS

Advances on the Genetics of Mendelian Idiopathic Epilepsies

(2010) Stéphanie Baulac et al.   CLINICS IN LABORATORY MEDICINE

Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12

(2010) José Morales-Corraliza et al.   EPILEPSIA