A Robust and Comprehensive Study of the Molecular and Genetic Basis of Neurodevelopmental Delay in a Sample of 3244 Patients, Evaluated by Exome Analysis in a Latin Population

<b>Background and Objectives</b>: Neurodevelopmental disorders (NDDs), including developmental delay (DD), autism spectrum disorder (ASD), intellectual disability (ID), attention-deficit/hyperactivity disorder (ADHD), and specific learning disorders, affect 15% of children and adolescents worldwide....

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Hlavní autoři:	Julian Lamilla, Taryn A. Castro-Cuesta, Paula Rueda-Gaitán, Laura Camila Rios Pinto, Diego Alejandro Rodríguez Gutiérrez, Yuri Natalia Sanchez Rubio, Carlos Estrada-Serrato, Olga Londoño, Cynthia Rucinski, Mauricio Arcos-Burgos, Mario Isaza-Ruget, Juan Javier López Rivera
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	MDPI AG 2025-02-01
Edice:	Diagnostics
Témata:	neurodevelopmental disorders whole exome sequencing genetic testing
On-line přístup:	https://www.mdpi.com/2075-4418/15/3/376
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