Fragile X Syndrome: Lessons Learned from the Most Translated Neurodevelopmental Disorder in Clinical Trials

Fragile X syndrome (FXS) is the leading genetic cause of autism spectrum disorder (ASD) and inherited intellectual disability (ID) worldwide. Preclinical successes in understanding the biology of FXS have led to numerous translational attempts in human clinical trials of therapeutics that target the...

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Detalles Bibliográficos
Autores principales: Duy, Phan Q., Budimirovic, Dejan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2017
Materias:
Regular Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382936/
https://www.ncbi.nlm.nih.gov/pubmed/28400977
http://dx.doi.org/10.1515/tnsci-2017-0002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382936/
https://www.ncbi.nlm.nih.gov/pubmed/28400977
http://dx.doi.org/10.1515/tnsci-2017-0002

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