Aberrant Splicing Events Associated to CDH23 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) analysis i...

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Detalles Bibliográficos
Autores principales: Valero, Rebeca, de Castro-Miró, Marta, Jiménez-Ochoa, Sofía, Rodríguez-Ezcurra, Juan José, Marfany, Gemma, Gonzàlez-Duarte, Roser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826400/
https://www.ncbi.nlm.nih.gov/pubmed/31546658
http://dx.doi.org/10.3390/genes10100732

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826400/
https://www.ncbi.nlm.nih.gov/pubmed/31546658
http://dx.doi.org/10.3390/genes10100732

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