Associated Papers
Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
Jiao JP et al.
Orphanet Journal of Rare Diseases, 2025
Christianson syndrome across the lifespan: genetic mutations and longitudinal study in children, adolescents, and adults.
Kavanaugh BC et al.
Journal of Medical Genetics, 2024
Christianson Syndrome across the Lifespan: An International Longitudinal Study in Children, Adolescents, and Adults.
Kavanaugh BC et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Case Report: Christianson Syndrome Caused by SLC9A6 Mutation: From Case to Genotype-Phenotype Analysis.
Lan Y et al.
Frontiers in Genetics, 2021
34987551 (PubMed )
Supplement: Table3.xlsx › Sheet1
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