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

10.1186/1471-2091-11-39

Saved in:

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
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

id	sg-nus-scholar.10635-174456
record_format	dspace
spelling	sg-nus-scholar.10635-1744562024-04-03T06:27:29Z Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2 Limviphuvadh, V Chua, L.L Rahim, R.A.B Eisenhaber, F Maurer-Stroh, S Adhikari, S. BIOLOGICAL SCIENCES 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 10.1186/1471-2091-11-39 BMC Biochemistry 11 1 39 2020-09-04T06:37:26Z 2020-09-04T06:37:26Z 2010 Article Limviphuvadh, V, Chua, L.L, Rahim, R.A.B, Eisenhaber, F, Maurer-Stroh, S, Adhikari, S. (2010). Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2. BMC Biochemistry 11 (1) : 39. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2091-11-39 14712091 https://scholarbank.nus.edu.sg/handle/10635/174456 BioMed Central Ltd. Unpaywall 20200831
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	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
spellingShingle	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 Limviphuvadh, V Chua, L.L Rahim, R.A.B Eisenhaber, F Maurer-Stroh, S Adhikari, S. Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
description	10.1186/1471-2091-11-39
author2	BIOLOGICAL SCIENCES
author_facet	BIOLOGICAL SCIENCES Limviphuvadh, V Chua, L.L Rahim, R.A.B Eisenhaber, F Maurer-Stroh, S Adhikari, S.
format	Article
author	Limviphuvadh, V Chua, L.L Rahim, R.A.B Eisenhaber, F Maurer-Stroh, S Adhikari, S.
author_sort	Limviphuvadh, V
title	Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
title_short	Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
title_full	Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
title_fullStr	Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
title_full_unstemmed	Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2
title_sort	similarity of molecular phenotype between known epilepsy gene lgi1 and disease candidate gene lgi2
publisher	BioMed Central Ltd.
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/174456
_version_	1795374337567490048

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

Similar Items