A recurrent mutation inDEPDC5predisposes to focal epilepsies in the French-Canadian population

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

(2013) Saeko Ishida et al.   NATURE GENETICS

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

(2013) Leanne M Dibbens et al.   NATURE GENETICS

A Tumor Suppressor Complex with GAP Activity for the Rag GTPases That Signal Amino Acid Sufficiency to mTORC1

(2013) L. Bar-Peled et al.   SCIENCE

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

Advances on the Genetics of Mendelian Idiopathic Epilepsies

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

A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11

(2008) Peter Kinirons et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A