Cargando…
Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report
BACKGROUND: Forkhead box protein 1 (FOXP1) (OMIM: 605515) at chromosomal region 3p14.1 plays an important regulatory role in cell development and functions by regulating genetic expression. Earlier studies have suggested that FOXP1, an oncogene, is capable of initiating tumorigenicity depending on t...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2021
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362507/ https://www.ncbi.nlm.nih.gov/pubmed/34447835 http://dx.doi.org/10.12998/wjcc.v9.i23.6858 |