Changes in Language Pathways in Tuberous Sclerosis Complex Patients with Autism
Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disease caused by loss of the TSC1 (encoding hamartin) or TSC2 (encoding tuberin) genes. Neurologic symptoms are common and varied in TSC and include epilepsy and behavioral conditions like autism spectrum disorders (ASD). Betw...
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| Format: | Others |
| Language: | en |
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Harvard University
2014
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| Online Access: | http://etds.lib.harvard.edu/hms/admin/view/45 http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407607 |