A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome

Recently, increasing numbers of rare pathogenic genetic variants have been identified that are associated with variably elevated risks of a range of neurodevelopmental outcomes, notably including Autism Spectrum Disorders (ASD), Schizophrenia Spectrum Disorders (SSD), and Intellectual Disability (ID...

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Detalles Bibliográficos
Autores principales: Fiksinski, Ania M., Hoftman, Gil D., Vorstman, Jacob A. S., Bearden, Carrie E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Expert Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812786/
https://www.ncbi.nlm.nih.gov/pubmed/36192458
http://dx.doi.org/10.1038/s41380-022-01783-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812786/
https://www.ncbi.nlm.nih.gov/pubmed/36192458
http://dx.doi.org/10.1038/s41380-022-01783-5

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