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. 2025 Feb;12(2):239-241.
doi: 10.1002/mdc3.14246. Epub 2024 Oct 24.

Causative Role of the SLC6A1 p.Asp451Gly Variant in a Patient with Combined Dystonia and Neurodevelopmental Disorder

Affiliations

Causative Role of the SLC6A1 p.Asp451Gly Variant in a Patient with Combined Dystonia and Neurodevelopmental Disorder

Luigi M Romito et al. Mov Disord Clin Pract. 2025 Feb.
No abstract available

Keywords: SLC6A1; autism; dystonia; epilepsy; sensory trick.

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References

    1. Carvill GL, McMahon JM, Schneider A, et al. Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic‐atonic seizures. Am J Hum Genet 2015;96:808–815. - PMC - PubMed
    1. Zhou Y, Danbolt NC. GABA and glutamate transporters in brain. Front Endocrinol (Lausanne) 2013;4:165. - PMC - PubMed
    1. Stefanski A, Perez‐Palma E, Brunger T, et al. SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis. Brain 2023;146:5198–5208. - PMC - PubMed
    1. Johannesen KM, Nielsen J, Sabers A, et al. The phenotypic presentation of adult individuals with SLC6A1‐related neurodevelopmental disorders. Front Neurosci 2023;17:1–7. - PMC - PubMed
    1. Bowling KM, Thompson ML, Amaral MD, et al. Genomic diagnosis for children with intellectual disability and/or developmental delay. Genome Med 2017;9:43. - PMC - PubMed

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