Journal article
BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes
Abstract
Coffin–Siris and Nicolaides–Baraitser syndromes (CSS and NCBRS) are Mendelian disorders caused by mutations in subunits of the BAF chromatin remodeling complex. We report overlapping peripheral blood DNA methylation epi-signatures in individuals with various subtypes of CSS (ARID1B, SMARCB1, and SMARCA4) and NCBRS (SMARCA2). We demonstrate that the degree of similarity in the epi-signatures of some CSS subtypes and NCBRS can be greater than …
Authors
Aref-Eshghi E; Bend EG; Hood RL; Schenkel LC; Carere DA; Chakrabarti R; Nagamani SCS; Cheung SW; Campeau PM; Prasad C
Journal
Nature Communications, Vol. 9, No. 1,
Publisher
Springer Nature
DOI
10.1038/s41467-018-07193-y
ISSN
2041-1723
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Abnormalities, MultipleChromatin Assembly and DisassemblyChromosomal Proteins, Non-HistoneDNA HelicasesDNA MethylationDNA-Binding ProteinsEpigenesis, GeneticEpigenomicsFaceFaciesFoot Deformities, CongenitalHand Deformities, CongenitalHumansHypotrichosisIntellectual DisabilityMicrognathismMutationNeckNuclear ProteinsSMARCB1 ProteinSyndromeTranscription Factors