Associated Papers
Electroencephalographic and Epilepsy Findings in ZNF711 Variants: A Case Series of Two Siblings.
Minerva M et al.
Neurology International, 2025
Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
Wang J et al.
European Journal of Human Genetics : Ejhg, 2022
Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.
van der Werf IM et al.
Gene, 2017
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