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Paper Details

INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.
Nat Commun
9
2022
C, INTS13, INTS13 variants, Integrator cleavage module, Integrator complex, OFD, OFD type 2, OFDs, Oral-facial-digital (OFD) syndromes, RNA Polymerase II, Xenopus, Xenopus embryos, autosomal recessive ciliopathy, cilia-related genes, ciliary genes, congenital disorders, cultured cells, developmental ciliopathies, digit anomalies, human, human cultured cells, malformations of the face and oral cavity, motile cilia anomalies, nascent RNA, recessive developmental ciliopathy
Author NameAffiliation
Barry MerrimanDavid Geffen School of Medicine, University of California Los Angeles
Barry MerrimanDavid Geffen School of Medicine, University of California Los Angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California Los Angeles
Stanley F NelsonDavid Geffen School of Medicine, University of California Los Angeles
Liang TongColumbia University
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