Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits

Autism is a highly heritable, heterogeneous, neurodevelopmental condition. Large-scale genetic studies, predominantly focussing on simplex families and clinical diagnoses of autism have identified hundreds of genes associated with autism. Yet, the contribution of these classes of genes to multiplex...

Descripción completa

Detalles Bibliográficos
Autores principales: More, Ravi Prabhakar, Warrier, Varun, Brunel, Helena, Buckingham, Clara, Smith, Paula, Allison, Carrie, Holt, Rosemary, Bradshaw, Charles R., Baron-Cohen, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575770/
https://www.ncbi.nlm.nih.gov/pubmed/36702863
http://dx.doi.org/10.1038/s41380-022-01938-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575770/
https://www.ncbi.nlm.nih.gov/pubmed/36702863
http://dx.doi.org/10.1038/s41380-022-01938-4

Ejemplares similares