channel, voltage-gated, type III, alpha subunit (SCN3A) is a protein that in humans is encoded by the SCN3A gene. Voltage-gated sodium channels are transmembrane...
8 KB (1,070 words) - 19:38, 22 December 2024
For instance, polymicrogyria has been associated with the channel gene SCN3A and the pump gene ATP1A3, among other genes that are not ion transporters...
14 KB (1,121 words) - 00:49, 22 December 2024
severity, and can be either unilateral or bilateral. The sodium channel SCN3A has been implicated in BPP. BPOP is located in the parasagittal and mesial...
28 KB (3,206 words) - 22:48, 3 September 2024
have to do with speech production. British Stammering Association FOXP2 SCN3A KE family Language disorder Manner of articulation Motor speech disorders...
16 KB (1,747 words) - 05:42, 23 May 2025
would not occur like in the human TSC. Variations within the sodium channel SCN3A, and Na+/K+,ATPase (ATP1A3), has been implicated in cortical malformations...
23 KB (2,929 words) - 07:32, 15 June 2024
ranging from mTORopathies (e.g. AKT3) to channelopathies (sodium channels, "SCN3A"). Patients with autism have overall higher levels of cortical gyrification...
37 KB (4,562 words) - 03:09, 7 February 2025
channel SCN3A in the development of the perisylvian areas, which maintain key language circuits- Broca and Wernicke Area. Patients with mutations in SCN3A had...
22 KB (2,423 words) - 11:35, 19 August 2024
are also observed. FOXP2 is known to regulate CNTNAP2, CTBP1, SRPX2 and SCN3A. FOXP2 downregulates CNTNAP2, a member of the neurexin family found in neurons...
53 KB (5,881 words) - 01:04, 30 September 2024
1 (IKCa1, SK4, KCNN4) KCa5.1 (Slo3, KCNU1) NALCN SCN1A; SCN2A; SCN2A2; SCN3A; SCN4A; SCN5A; SCN7A; SCN8A; SCN9A; SCN10A; SCN11A SLC9A10; SLC9A11 CNGA1;...
19 KB (1,692 words) - 03:53, 29 November 2023
Q07699 14370 SCN2A HGNC:10588 Q99250 14371 SCN2B HGNC:10589 O60939 14372 SCN3A HGNC:10590 Q9NY46 14373 SCN3B HGNC:20665 Q9NY72 14374 SCN4A HGNC:10591 P35499...
282 KB (17 words) - 09:28, 10 February 2025
inherited febrile seizures, epilepsy, and autism spectrum disorder Nav1.3 SCN3A Central neurons, peripheral neurons and cardiac myocytes epilepsy, pain...
35 KB (3,706 words) - 22:39, 19 February 2025
inherited febrile seizures, epilepsy, and autism spectrum disorder Nav1.3 SCN3A Central neurons, peripheral neurons and cardiac myocytes epilepsy, pain...
52 KB (5,625 words) - 19:57, 23 May 2025
N, Fukushima K, Ueki Y, et al. (2001). "Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus". Gene. 264 (1): 113–22...
10 KB (1,270 words) - 01:31, 29 April 2025
J. D.; Meisler, M. H. (2003-02-01). "Sodium channels SCN1A, SCN2A and SCN3A in familial autism". Molecular Psychiatry. 8 (2): 186–194. doi:10.1038/sj...
22 KB (2,421 words) - 04:00, 30 January 2025
Doan, Ryan N.; Anttonen, Anna-Kaisa (September 5, 2018). "Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development"...
10 KB (1,088 words) - 08:46, 3 December 2023
systems Rudolf Podgornik Ryanodine receptor 2 S-layer SCN10A SCN1B SCN2B SCN3A SCN3B SCN4B SCN7A SCN8A SCNN1A SCNN1B SCNN1D SCNN1G SIGLEC SK3 SK channel...
15 KB (1,545 words) - 18:32, 17 August 2024