An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
Cameli, Cinzia, Viggiano, Marta, Rochat, Magali J., Maresca, Alessandra, Caporali, Leonardo, Fiorini, Claudio, Palombo, Flavia, Magini, Pamela, Duardo, Renée C., Ceroni, Fabiola, Scaduto, Maria C., Posar, Annio, Seri, Marco, Carelli, Valerio, Visconti, Paola, Bacchelli, Elena, Maestrini, Elena
Published in Journal of cellular and molecular medicine (01.03.2021)
Published in Journal of cellular and molecular medicine (01.03.2021)
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