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An increased burden of rare exonic variants in NRXN1 microd..:
Cameli, Cinzia
;
Viggiano, Marta
;
Rochat, Magali J.
...
Journal of Cellular and Molecular Medicine. 25 (2021) 5 - p. 2459-2470 , 2021
Link:
https://doi.org/10.1111/jcmm.16161
RT Journal T1
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_jcmm.16161&Exemplar=1&LAN=DE A1 Cameli, Cinzia A1 Viggiano, Marta A1 Rochat, Magali J. A1 Maresca, Alessandra A1 Caporali, Leonardo A1 Fiorini, Claudio A1 Palombo, Flavia A1 Magini, Pamela A1 Duardo, Renée C. A1 Ceroni, Fabiola A1 Scaduto, Maria C. A1 Posar, Annio A1 Seri, Marco A1 Carelli, Valerio A1 Visconti, Paola A1 Bacchelli, Elena A1 Maestrini, Elena PB Wiley YR 2021 SN 1582-1838 SN 1582-4934 JF Journal of Cellular and Molecular Medicine VO 25 IS 5 SP 2459 OP 2470 LK http://dx.doi.org/https://doi.org/10.1111/jcmm.16161 DO https://doi.org/10.1111/jcmm.16161 SF ELIB - SuUB Bremen
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