Aberrant Splicing Events Associated to <i>CDH23</i> Noncanonical Splice Site Mutations in a Proband with Atypical Usher Syndrome 1
Aims: The aim of this study was the genetic diagnosis by next generation sequencing (NGS) of a patient diagnosed with Usher syndrome type 2 and the functional evaluation of the identified genetic variants to establish a phenotype−genotype correlation. Methods: Whole exome sequencing (WES)...
Main Authors: | Rebeca Valero, Marta de Castro-Miró, Sofía Jiménez-Ochoa, Juan José Rodríguez-Ezcurra, Gemma Marfany, Roser Gonzàlez-Duarte |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2019-09-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/10/10/732 |
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