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Nature (London), ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | Index Medicus | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
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Journal of autism and developmental disorders, ISSN 0162-3257, 2/2009, Volume 39, Issue 2, pp. 223 - 230
GABRA2 | GABRB3 | Pediatrics | GABRA1 | Autism | Brain | Child and School Psychology | Psychology | GABRA3 | Public Health/Gesundheitswesen | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | brain | autism
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Basal ganglia, ISSN 2210-5336, 03/2018, Volume 11, pp. 4 - 7
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Pharmacognosy journal, 08/2020, Volume 12, Issue 4
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Schizophrenia research, ISSN 0920-9964, 06/2020, Volume 220, pp. 29 - 37
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Brain (London, England : 1878), ISSN 0006-8950, 08/2018, Volume 141, Issue 8, pp. 2392 - 2405
GABRA2 | GABRB3 | GABA | Epileptic encephalopathy | receptor | GABRA5 | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Patch-Clamp Techniques | gamma-Aminobutyric Acid - metabolism | Humans | Receptors, GABA-A - genetics | HEK293 Cells | Epilepsies, Myoclonic - physiopathology | Epilepsy - genetics | Developmental Disabilities - genetics | Receptors, GABA-A - metabolism | Mutation | Child | Epilepsies, Myoclonic - genetics | Index Medicus | Abridged Index Medicus | Editor's Choice | GABAA receptor | Original | epileptic encephalopathy
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Brain (London, England : 1878), ISSN 0006-8950, 10/2019, Volume 142, Issue 10, pp. 3028 - 3044
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Cerebral cortex (New York, N.Y. 1991), ISSN 1047-3211, 03/2015, Volume 25, Issue 3, pp. 631 - 645
GABRB3 | GABA | Cerebral cortex | inhibitory interneurons | neurodevelopmental disorders | DLX genes | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Gene Expression | Basic Helix-Loop-Helix Transcription Factors - genetics | Neocortex - embryology | Humans | Glutamate Decarboxylase - genetics | Oligodendrocyte Transcription Factor 2 | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Interneurons - metabolism | GABAergic Neurons - cytology | Cell Division | Interneurons - cytology | GABAergic Neurons - metabolism | Calbindin 2 - genetics | Real-Time Polymerase Chain Reaction | Index Medicus | cerebral cortex
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Neuropediatrics, ISSN 0174-304X, 06/2018, Volume 49, Issue 3, pp. 204 - 208
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GABAA receptor β3 subunit mutation D120N causes Lennox–Gastaut syndrome in knock-in mice
Brain Communications, ISSN 2632-1297, 01/2020, Volume 2, Issue 1, pp. fcaa028 - fcaa028
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