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Ionotropic GABA and glutamate receptor mutations and human neurologic diseases

Ionotropic GABA and glutamate receptor mutations and human neurologic diseases

10.1124/mol.115.097998

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Bibliographic Details
Main Authors: Yuan, H, Low, C.-M, Moody, O.A, Jenkins, A, Traynelis, S.F
Other Authors: PHARMACOLOGY
Format: Others
Published: American Society for Pharmacology and Experimental Therapeutics 2020
Subjects:
4 aminobutyric acid
4 aminobutyric acid A receptor
alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid
delta opiate receptor
glutamate receptor
kainic acid
n methyl dextro aspartic acid
4 aminobutyric acid receptor
central nervous system agents
ionotropic receptor
addiction
autism
functional genomics
gene mutation
genetic association
human
neurologic disease
next generation sequencing
priority journal
schizophrenia
Short Survey
binding site
chemistry
genetic predisposition
genetic variability
genetics
metabolism
Nervous System Diseases
protein tertiary structure
Binding Sites
Central Nervous System Agents
Genetic Predisposition to Disease
Genetic Variation
Humans
Protein Structure, Tertiary
Receptors, GABA
Receptors, Ionotropic Glutamate
Online Access:https://scholarbank.nus.edu.sg/handle/10635/183883
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Institution: National University of Singapore
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Internet

https://scholarbank.nus.edu.sg/handle/10635/183883

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