Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss

PURPOSE: Hearing loss (HL) is the most common sensory disorder in children. Prompt molecular diagnosis may guide screening and management, especially in syndromic cases when HL is the single presenting feature. Exome sequencing (ES) is an appealing diagnostic tool for HL as the genetic causes are hi...

Descripción completa

Detalles Bibliográficos
Autores principales: Sheppard, Sarah, Biswas, Sawona, Li, Mindy H., Jayaraman, Vijayakumar, Slack, Ian, Romasko, Edward J., Sasson, Ariella, Brunton, Joshua, Rajagopalan, Ramakrishnan, Sarmady, Mahdi, Abrudan, Jenica L., Jairam, Sowmya, DeChene, Elizabeth T., Ying, Xiahoan, Choi, Jiwon, Wilkens, Alisha, Raible, Sarah E., Scarano, Maria I., Santani, Avni, Pennington, Jeffrey W., Luo, Minjie, Conlin, Laura K., Devkota, Batsal, Dulik, Matthew C., Spinner, Nancy B., Krantz, Ian D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295269/
https://www.ncbi.nlm.nih.gov/pubmed/29907799
http://dx.doi.org/10.1038/s41436-018-0004-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295269/
https://www.ncbi.nlm.nih.gov/pubmed/29907799
http://dx.doi.org/10.1038/s41436-018-0004-x

Ejemplares similares