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

• Main Authors: Limviphuvadh, V, Chua, L.L, Rahim, R.A.B, Eisenhaber, F, Maurer-Stroh, S, Adhikari, S.
• Other Authors: BIOLOGICAL SCIENCES
• Format: Article
• Published: BioMed Central Ltd. 2020
• Subjects: leucine rich glioma inactivated 1 protein; leucine rich glioma inactivated 2 protein; mutant protein; regulator protein; unclassified drug; LGI1 protein, human; LGI2 protein, human; protein; article; cellular distribution; controlled study; convergent evolution; endoplasmic reticulum; epilepsy; extracellular space; gene mapping; gene mutation; glycosylation; human; human cell; nucleotide sequence; phenotype; protein domain; protein secretion; protein structure; single nucleotide polymorphism; wild type; chemistry; classification; focal epilepsy; genetics; missense mutation; phylogeny; protein tertiary structure; temporal lobe epilepsy; Epilepsies, Partial; Epilepsy, Temporal Lobe; Humans; Mutation, Missense; Phenotype; Phylogeny; Polymorphism, Single Nucleotide; Protein Structure, Tertiary; Proteins
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/174456
• Institution: National University of Singapore

10.1186/1471-2091-11-39