Exome Evaluation of Autism-Associated Genes in Amazon American Populations

Autism spectrum disorder is a neurodevelopmental disorder, affecting one in 160 children worldwide. The causes of autism are still poorly understood, but research shows the relevance of genetic factors in its pathophysiology, including the CHD8, SCN2A, FOXP1 and SYNGAP1 genes. Information about the...

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Detalles Bibliográficos
Autores principales: da Costa, Giovana E., Fernandes, Giordane L., Rodrigues, Juliana C. G., da V. B. Leal, Diana F., Pastana, Lucas F., Pereira, Esdras E. B., Assumpção, Paulo P., Burbano, Rommel M. R., dos Santos, Sidney E. B., Guerreiro, João F., Fernandes, Marianne R., dos Santos, Ney P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871861/
https://www.ncbi.nlm.nih.gov/pubmed/35205412
http://dx.doi.org/10.3390/genes13020368

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871861/
https://www.ncbi.nlm.nih.gov/pubmed/35205412
http://dx.doi.org/10.3390/genes13020368

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