Phenotypic and Molecular Convergence of 2q23.1 Deletion Syndrome with Other Neurodevelopmental Syndromes Associated with Autism Spectrum Disorder

Roughly 20% of autism spectrum disorders (ASD) are syndromic with a well-established genetic cause. Studying the genes involved can provide insight into the molecular and cellular mechanisms of ASD. 2q23.1 deletion syndrome (causative gene, MBD5) is a recently identified genetic neurodevelopmental d...

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Detalles Bibliográficos
Autores principales: Mullegama, Sureni V., Alaimo, Joseph T., Chen, Li, Elsea, Sarah H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425039/
https://www.ncbi.nlm.nih.gov/pubmed/25853262
http://dx.doi.org/10.3390/ijms16047627

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425039/
https://www.ncbi.nlm.nih.gov/pubmed/25853262
http://dx.doi.org/10.3390/ijms16047627

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