PTCHD1: Identification and Neurodevelopmental Contributions of an Autism Spectrum Disorder and Intellectual Disability Susceptibility Gene

Over the last one and a half decades, copy number variation and whole-genome sequencing studies have illuminated the considerable genetic heterogeneity that underlies the etiologies of autism spectrum disorder (ASD) and intellectual disability (ID). These investigations support the idea that ASD may...

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Detalles Bibliográficos
Autores principales: Pastore, Stephen F., Ko, Sangyoon Y., Frankland, Paul W., Hamel, Paul A., Vincent, John B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953913/
https://www.ncbi.nlm.nih.gov/pubmed/35328080
http://dx.doi.org/10.3390/genes13030527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953913/
https://www.ncbi.nlm.nih.gov/pubmed/35328080
http://dx.doi.org/10.3390/genes13030527

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