Homo sapiens cDNA FLJ75537 partial cds, highly similar to Homo sapiens - Nucleotide

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Pathogenic gating pore current conducted by autism-related mutations in the Na(V)1.2 brain sodium channel. [Proc Natl Acad Sci U S A. 2024]
Pathogenic gating pore current conducted by autism-related mutations in the Na(V)1.2 brain sodium channel.
Eltokhi A, Lundstrom BN, Li J, Zweifel LS, Catterall WA, Gamal El-Din TM. Proc Natl Acad Sci U S A. 2024 Apr 9; 121(15):e2317769121. Epub 2024 Apr 2.
Distinctive In Vitro Phenotypes in iPSC-Derived Neurons From Patients With Gain- and Loss-of-Function SCN2A Developmental and Epileptic Encephalopathy. [J Neurosci. 2024]
Distinctive In Vitro Phenotypes in iPSC-Derived Neurons From Patients With Gain- and Loss-of-Function SCN2A Developmental and Epileptic Encephalopathy.
Mao M, Mattei C, Rollo B, Byars S, Cuddy C, Berecki G, Heighway J, Pachernegg S, Menheniott T, Apted D, et al. J Neurosci. 2024 Feb 21; 44(8). Epub 2024 Feb 21.
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. [Eur J Hum Genet. 2024]
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.
Panagiotakaki E, Tiziano FD, Mikati MA, Vijfhuizen LS, Nicole S, Lesca G, Abiusi E, Novelli A, Di Pietro L, I.B.AHC Consortium, et al. Eur J Hum Genet. 2024 Feb; 32(2):224-231. Epub 2023 Dec 14.

Homo sapiens cDNA FLJ75537 partial cds, highly similar to Homo sapiens sodium ch...
Homo sapiens cDNA FLJ75537 partial cds, highly similar to Homo sapiens sodium channel, voltage-gated, type II, alpha 2 (SCN2A2), mRNA
gi|158260334|dbj|AK289656.1|

Nucleotide
Human dystrophin gene, exon 44
Human dystrophin gene, exon 44
gi|181884|gb|M81257.1|HUMDYSTRO

Nucleotide
Mus musculus 6 days neonate head cDNA, RIKEN full-length enriched library, clone...
Mus musculus 6 days neonate head cDNA, RIKEN full-length enriched library, clone:5430419D17 product:hypothetical CUB domain containing protein, full insert sequence
gi|12856501|dbj|AK017319.1|

Nucleotide
LOC130058858 [Homo sapiens]
LOC130058858 [Homo sapiens]
Gene ID:130058858

Gene
LOC130058853 [Homo sapiens]
LOC130058853 [Homo sapiens]
Gene ID:130058853

Gene

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Nucleotide