Associated Papers
A Boy with a Novel Variant in TCF20: An Expanded Phenotype and a Brief Review of the Literature.
Ziveri D et al.
Children (basel, Switzerland), 2025
Regulation of Dendrite and Dendritic Spine Formation by TCF20.
Vinci E et al.
Journal of Neurochemistry, 2025
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Zhang Y et al.
Molecular Neurobiology, 2021
Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature.
Torti E et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Vetrini F et al.
Genome Medicine, 2019
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