An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder-Reference-Cited by-同舟云学术

An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder

Published:2021-01-21 Issue:5 Volume:25 Page:2459-2470
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cellular Molecular Medi

Author:

Cameli Cinzia¹,Viggiano Marta¹,Rochat Magali J.²,Maresca Alessandra³,Caporali Leonardo³,Fiorini Claudio³⁴,Palombo Flavia³,Magini Pamela⁵,Duardo Renée C.¹,Ceroni Fabiola⁶,Scaduto Maria C.²,Posar Annio²⁴,Seri Marco⁵,Carelli Valerio³⁴,Visconti Paola²,Bacchelli Elena¹^ORCID,Maestrini Elena¹

Affiliation:

1. Department of Pharmacy and Biotechnology University of Bologna Bologna Italy

2. UOSI Disturbi dello Spettro Autistico, Ospedale Bellaria di Bologna IRCCS Istituto delle Scienze Neurologiche di Bologna Bologna40139Italy

3. IRCCS Istituto delle Scienze Neurologiche di Bologna UOC Clinica Neurologica Bologna Italia

4. Department of Biomedical and Neuromotor Sciences (DIBINEM) University of Bologna Bologna Italy

5. Unit of Medical Genetics Department of Medical and Surgical Sciences Policlinico St. Orsola‐Malpighi HospitalUniversity of Bologna Bologna Italy

6. Faculty of Health and Life Sciences Oxford Brookes University Oxford UK

Funder

Università di Bologna

Publisher

Wiley

Subject