Profiling Genome-Wide DNA Methylation in Children with Autism Spectrum Disorder and in Children with Fragile X Syndrome

Autism spectrum disorder (ASD) is an early onset, developmental disorder whose genetic cause is heterogeneous and complex. In total, 70% of ASD cases are due to an unknown etiology. Among the monogenic causes of ASD, fragile X syndrome (FXS) accounts for 2–4% of ASD cases, and 60% of individuals wit...

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Detalles Bibliográficos
Autores principales: Jasoliya, Mittal, Gu, Jianlei, AlOlaby, Reem R., Durbin-Johnson, Blythe, Chedin, Frederic, Tassone, Flora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602177/
https://www.ncbi.nlm.nih.gov/pubmed/36292679
http://dx.doi.org/10.3390/genes13101795

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602177/
https://www.ncbi.nlm.nih.gov/pubmed/36292679
http://dx.doi.org/10.3390/genes13101795

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