Skip to Main Content

Paper Details

Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report.
J Pers Med
0
2022
ASD, Autism, Autism spectrum disorder, CDLS, CUL4, Cornelia De Lange Syndrome, DCAF1, DDB1, E3 ligase complex, E3 ubiquitin ligase, Intellectual Disability, X- linked intellectual disability, X-linked intellectual disability, autism, autistic features, c.137, candidate gene, exon 4, hypospadias, intellectual disabilities, intellectual disability, microcephaly, mitochondrial genes, neurodevelopmental disorders, patient, pulmonary vascular anomaly, small stature
Author NameAffiliation
Patricia Porter-GillArkansas Children's Research Institute
Patricia Porter-GillArkansas Children's Research Institute
  • 1 - 2

Datasets

Release 1.2