Mutations in DEPDC5 cause familial focal epilepsy with variable foci

WNTs in synapse formation and neuronal circuitry

(2012) Mikyoung Park et al.   EMBO JOURNAL

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

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance

(2010) D. E. Crompton et al.   BRAIN

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

(2010) José Morales-Corraliza et al.   EPILEPSIA

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

(2009) Helen V. Firth et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Electrochemical cues regulate assembly of the Frizzled/Dishevelled complex at the plasma membrane during planar epithelial polarization

(2009) Matias Simons et al.   NATURE CELL BIOLOGY

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

(2009) Ingo Helbig et al.   NATURE GENETICS

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

(2008) Andrew J Sharp et al.   NATURE GENETICS