An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
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E. Bacchelli | E. Maestrini | V. Carelli | A. Posar | A. Maresca | L. Caporali | M. Seri | P. Magini | Flavia Palombo | P. Visconti | F. Ceroni | M. J. Rochat | Claudio Fiorini | M. Scaduto | Cinzia Cameli | Marta Viggiano | Renée C Duardo
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