Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

The genetic heterogeneity of congenital hearing disorders makes molecular diagnosis expensive and time-consuming using conventional techniques such as Sanger sequencing of DNA. In order to design an appropriate strategy of molecular diagnosis in the Algerian population, we explored the diversity of...

Descripción completa

Detalles Bibliográficos
Autores principales: Ammar-Khodja, Fatima, Bonnet, Crystel, Dahmani, Malika, Ouhab, Sofiane, Lefèvre, Gaelle M, Ibrahim, Hassina, Hardelin, Jean-Pierre, Weil, Dominique, Louha, Malek, Petit, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444160/
https://www.ncbi.nlm.nih.gov/pubmed/26029705
http://dx.doi.org/10.1002/mgg3.131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444160/
https://www.ncbi.nlm.nih.gov/pubmed/26029705
http://dx.doi.org/10.1002/mgg3.131

Ejemplares similares