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- W2975830090 abstract "Objective: Early infantile epileptic encephalopathy type11 (EIEE) generally known as an autosomal dominant inherited disease caused by the voltage-gated sodium channel neuronal type 2 alpha subunit (Navα1.2) encoded by the SCN2A gene mutations. The clinic of the disease is variable. Herein we report the second case with a homozygous missense mutation of the SCN2A gene (c.1588 G>T).
 Material and methods: NGS gene panel including the SCN2A gene from genomic DNA extracted from peripheral blood using a commercially available kit and quantified using standard methods. Illumina miseq analysis platform was used for this purpose, we performed analysis of coding regions and exon-intron boundaries and the data was analyzed by IGV.
 Results: The results confirmed by sanger sequencing show us an SCN2A (NM_001040142) c.1588 G>T homozygote mutation.
 Conclusion: This shows us more clinical and molecular studies need for SCN2A associated disease pathogenesis" @default.
- W2975830090 created "2019-10-03" @default.
- W2975830090 creator A5054331503 @default.
- W2975830090 date "2019-09-24" @default.
- W2975830090 modified "2023-09-24" @default.
- W2975830090 title "Homozygous SCN2A gene mutation causing early infantile epileptic encephalopathy: The second case in literature" @default.
- W2975830090 doi "https://doi.org/10.36472/msd.v6i9.302" @default.
- W2975830090 hasPublicationYear "2019" @default.
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