Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet–Biedl and Usher Syndromes

Aim: To identify disease-causing mutations in four Lebanese families: three families with Bardet–Biedl and one family with Usher syndrome (BBS and USH respectively), using next generation sequencing (NGS). Methods: We applied targeted NGS in two families and whole exome sequencing (WES) in two other...

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Detalles Bibliográficos
Autores principales: Jaffal, Lama, Joumaa, Wissam H, Assi, Alexandre, Helou, Charles, Cherfan, George, Zibara, Kazem, Audo, Isabelle, Zeitz, Christina, El Shamieh, Said
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947157/
https://www.ncbi.nlm.nih.gov/pubmed/31888296
http://dx.doi.org/10.3390/genes10121047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947157/
https://www.ncbi.nlm.nih.gov/pubmed/31888296
http://dx.doi.org/10.3390/genes10121047

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