Risk factors for the development of autism spectrum disorder in children with tuberous sclerosis complex: protocol for a systematic review

BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant condition, caused by mutations in either the TSC1 or TSC2 gene. It has widespread systemic manifestations and is associated with significant neurological morbidity. In addition to seizures and cerebral pathology including cortical...

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Detalles Bibliográficos
Autores principales: Mitchell, Rebecca, Barton, Sarah, Harvey, A. Simon, Williams, Katrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341363/
https://www.ncbi.nlm.nih.gov/pubmed/28270230
http://dx.doi.org/10.1186/s13643-017-0448-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341363/
https://www.ncbi.nlm.nih.gov/pubmed/28270230
http://dx.doi.org/10.1186/s13643-017-0448-0

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