Dystrophin deficiency leads to dysfunctional glutamate clearance in iPSC derived astrocytes
Author:
Funder
KU Leuven
Publisher
Springer Science and Business Media LLC
Subject
Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health
Link
http://www.nature.com/articles/s41398-019-0535-1.pdf
Reference90 articles.
1. Daoud, F. et al. Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions. PLoS ONE 4, e6574 (2008).
2. Ricotti, V. et al. Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations. Dev. Med. Child Neurol. https://doi.org/10.1111/dmcn.12922 (2015).
3. Banihani, R. et al. Cognitive and neurobehavioral profile in boys with duchenne muscular dystrophy. J. Child Neurol. 30, 1472–1482 (2015).
4. Taylor, P. J. et al. Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy. PLoS ONE 5, e8803 (2010).
5. Pane, M. et al. Attention deficit hyperactivity disorder and cognitive function in duchenne muscular dystrophy: phenotype-genotype correlation. J. Pediatr. 161, 705–709.e1 (2012).
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