Synaptic vesicle dynamic changes in a model of fragile X

BACKGROUND: Fragile X syndrome (FXS) is a single-gene disorder that is the most common heritable cause of intellectual disability and the most frequent monogenic cause of autism spectrum disorders (ASD). FXS is caused by an expansion of trinucleotide repeats in the promoter region of the fragile X m...

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Detalles Bibliográficos
Autores principales: Broek, Jantine A. C., Lin, Zhanmin, de Gruiter, H. Martijn, van ‘t Spijker, Heleen, Haasdijk, Elize D., Cox, David, Ozcan, Sureyya, van Cappellen, Gert W. A., Houtsmuller, Adriaan B., Willemsen, Rob, de Zeeuw, Chris I., Bahn, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772588/
https://www.ncbi.nlm.nih.gov/pubmed/26933487
http://dx.doi.org/10.1186/s13229-016-0080-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772588/
https://www.ncbi.nlm.nih.gov/pubmed/26933487
http://dx.doi.org/10.1186/s13229-016-0080-1

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