Associated Papers
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
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.
Kamal N et al.
European Journal of Medical Genetics, 2022
Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features.
Kameyama S et al.
Journal of Human Genetics, 2022
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