Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report

Autism spectrum disorder (ASD) comprises a heterogeneous group of neurodevelopmental disorders and occurs in all racial, ethnic, and socioeconomic groups. Cutting-edge technologies are contributing to understanding genetic underpinnings in ASD. The reported patient is a 32-year-old male and as an in...

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Detalles Bibliográficos
Autores principales: Clothier, Jeffery L., Grooms, Amy N., Porter-Gill, Patricia A., Gill, Pritmohinder S., Schaefer, G. Bradley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224943/
https://www.ncbi.nlm.nih.gov/pubmed/35743672
http://dx.doi.org/10.3390/jpm12060886

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224943/
https://www.ncbi.nlm.nih.gov/pubmed/35743672
http://dx.doi.org/10.3390/jpm12060886

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