Associated Papers
Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability.
De Hayr L et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025
Biallelic variants in GTF3C3 encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafish.
Abdel-Hamid MS et al.
Brain Communications, 2025
Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families.
AlAbdi L et al.
Nature Communications, 2023
37644014 (PubMed )
Supplement: 41467_2023_40909_MOESM10_ESM.xlsx › Sheet1
Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics.
Maddirevula S et al.
Genome Biology, 2020
32552793 (PubMed )
Supplement: 13059_2020_2053_MOESM3_ESM.xlsx › Table_S2
Correction to: Expanding the genetic heterogeneity of intellectual disability.
Anazi S et al.
Human Genetics, 2018
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