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

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

10.1186/1471-2091-11-39

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Bibliographic Details
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
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Institution:	National University of Singapore

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Summary:	10.1186/1471-2091-11-39