Shared Neurodevelopmental Perturbations Can Lead to Intellectual Disability in Individuals with Distinct Rare Chromosome Duplications

Chromosomal duplications are associated with a large group of human diseases that arise mainly from dosage imbalance of genes within the rearrangements. Phenotypes range widely but are often associated with global development delay, intellectual disability, autism spectrum disorders, and multiple co...

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Detalles Bibliográficos
Autores principales: Corrêa, Thiago, Santos-Rebouças, Cíntia B., Mayndra, Maytza, Schinzel, Albert, Riegel, Mariluce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146713/
https://www.ncbi.nlm.nih.gov/pubmed/33922640
http://dx.doi.org/10.3390/genes12050632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146713/
https://www.ncbi.nlm.nih.gov/pubmed/33922640
http://dx.doi.org/10.3390/genes12050632

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