INTS1

Publications

Krall M et al. Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies. Eur J Hum Genet. 2019;27(4):582-593. PMID: 30622326.

Oegema R et al. Human mutations in integrator complex subunits link transcriptome integrity to brain development. PLoS Genet. 2017;13(5):e1006809. PMID: 28542170.

Zhang X et al. Biallelic INTS1 Mutations Cause a Rare Neurodevelopmental Disorder in Two Chinese Siblings. J Mol Neurosci. 2020;70(1):1-8. PMID: 31428919.