bms204352 has been researched along with Abnormalities, Autosome in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andres, C; Belhadj, A; Briault, S; Cahard, D; Chaabouni, H; Colleaux, L; Constant, J; Elia, M; Guérin, P; Halayem, M; Holbert, S; Laumonnier, F; Le Guennec, JY; M'rad, R; Molinari, F; Persico, AM; Roger, S; Romano, V | 1 |
1 other study(ies) available for bms204352 and Abnormalities, Autosome
| Article | Year |
|---|---|
Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.
Topics: Autistic Disorder; Child; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Artificial, Bacterial; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 9; Cloning, Molecular; DNA Mutational Analysis; Humans; In Situ Hybridization, Fluorescence; Indoles; Intellectual Disability; Large-Conductance Calcium-Activated Potassium Channel alpha Subunits; Male; Reverse Transcriptase Polymerase Chain Reaction; Synaptic Transmission; Translocation, Genetic | 2006 |