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An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
Cameli C, Viggiano M, Rochat MJ, Maresca A, Caporali L, Fiorini C, Palombo F, Magini P, Duardo RC, Ceroni F, Scaduto MC, Posar A, Seri M, Carelli V, Visconti P, Bacchelli E, Maestrini E. Cameli C, et al. Among authors: visconti p. J Cell Mol Med. 2021 Mar;25(5):2459-2470. doi: 10.1111/jcmm.16161. Epub 2021 Jan 21. J Cell Mol Med. 2021. PMID: 33476483 Free PMC article.
Autism in 2016: the need for answers.
Posar A, Visconti P. Posar A, et al. Among authors: visconti p. J Pediatr (Rio J). 2017 Mar-Apr;93(2):111-119. doi: 10.1016/j.jped.2016.09.002. Epub 2016 Nov 9. J Pediatr (Rio J). 2017. PMID: 27837654 Free article. Review.
Authors' reply: "Autism in 2016: additional discovery".
Posar A, Visconti P. Posar A, et al. Among authors: visconti p. J Pediatr (Rio J). 2017 May-Jun;93(3):309-310. doi: 10.1016/j.jped.2016.12.002. Epub 2016 Dec 28. J Pediatr (Rio J). 2017. PMID: 28039733 Free article. No abstract available.
320 results