| Literature DB >> 30101418 |
Meera E Modi1, Mustafa Sahin1.
Abstract
Rare genetically defined neurodevelopmental disorders with increased risk of autism have recently become an entry point for autism-related drug discovery. Through exploration of downstream effects of the pathological mutations, specific mechanistic pathways have been identified as dysregulated. The identification of shared mechanisms across forms of autism opens the door for the development of novel "mechanism-based therapeutics." However, confidence in the therapeutic mechanism does not diminish the need for well-designed clinical trials.Entities:
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Year: 2018 PMID: 30101418 PMCID: PMC6175613 DOI: 10.1002/cpt.1181
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875