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...

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Detalles Bibliográficos
Autores principales: Lin, Shuang-Zhu, Zhou, Xin-Yu, Wang, Wan-Qi, Jiang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
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

Internet

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

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