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Delving into the genetic causes of language impairment in a case of partial deletion of NRXN1

Author:
Benítez Burraco, AntonioUniovi authority; Jiménez Romero, M. Salud; Fernández Urquiza, MaiteUniovi authority
Publication date:
2022
Publisher version:
http://dx.doi.org/10.1159/000524710
Citación:
Molecular Syndromology (2022); doi:10.1159/000524710
URI:
http://hdl.handle.net/10651/65452
ISSN:
1661-8769; 1661-8777
DOI:
10.1159/000524710
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