Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness

How the Genetics of Deafness Illuminates Auditory Physiology

(2011) Guy P. Richardson et al.   Annual Review of Physiology

Audiogenic seizure proneness requires the contribution of two susceptibility loci in mice

(2011) M. Catharine Jawahar et al.   NEUROGENETICS

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

(2011) P. Striano et al.   NEUROLOGY

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

(2011) Nikoletta Charizopoulou et al.   Nature Communications

LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs

(2011) Eija H. Seppälä et al.   PLoS Genetics

Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2

(2010) Vachiranee Limviphuvadh et al.   BMC BIOCHEMISTRY

Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice

(2010) Elodie Chabrol et al.   BRAIN

Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability

(2010) Y. Eugene Yu et al.   HUMAN MOLECULAR GENETICS

Adam22 Is a Major Neuronal Receptor for Lgi4-Mediated Schwann Cell Signaling

(2010) E. Ozkaynak et al.   JOURNAL OF NEUROSCIENCE

Disruption of LGI1–linked synaptic complex causes abnormal synaptic transmission and epilepsy

(2010) Yuko Fukata et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IS LGI2 THE CANDIDATE GENE FOR PARTIAL EPILEPSY WITH PERICENTRAL SPIKES?

(2010) VACHIRANEE LIMVIPHUVADH et al.   Journal of Bioinformatics and Computational Biology

Positive association between benign familial infantile convulsions and LGI4

(2009) Atsushi Ishii et al.   BRAIN & DEVELOPMENT

Quiet as a mouse: dissecting the molecular and genetic basis of hearing

(2008) Steve D. M. Brown et al.   NATURE REVIEWS GENETICS