Ionotropic GABA and glutamate receptor mutations and human neurologic diseases

• المؤلفون الرئيسيون: Yuan, H, Low, C.-M, Moody, O.A, Jenkins, A, Traynelis, S.F
• مؤلفون آخرون: PHARMACOLOGY
• التنسيق: Others
• منشور في: American Society for Pharmacology and Experimental Therapeutics 2020
• الموضوعات: 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
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/183883
• المؤسسة: National University of Singapore

10.1124/mol.115.097998