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
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.
Papuc SM et al.
European Journal of Human Genetics : Ejhg, 2019
30552426 (PubMed )
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