Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Overview of attention for article published in Nature Genetics, August 2022

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RFX3 is also an autism gene implicated through rare variant burden (www.nature.com/articles/s41...) and a regulator of activity-dependent transcription of immediate early genes (IEGs) (www.biorxiv.org/content/10.1...).

12/ Fu JM, Satterstrom FK, Peng M, et al. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54(9):1320–1331. www.nature.com/articles/s41...

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