Sara Selig
0000-0001-5759-9948
3 papers found
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ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
The aberrant epigenome ofDNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
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