Repositorio Institucional de la Universidad de Oviedo

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

Author:

Benítez Burraco, Antonio; Jiménez Romero, M. Salud; Fernández Urquiza, Maite

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