Associated Papers
[Clinical features and molecular pathogenesis of neurodevelopmental disorder with impaired speech and hyperkinetic movements associated with ZNF142 gene variants].
Xu Y et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2025
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.
Mir A et al.
Molecular Genetics & Genomic Medicine, 2023
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Christensen MB et al.
Clinical Genetics, 2022
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