Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper

BACKGROUND: Hearing loss (HL) is a highly prevalent heterogeneous deficiency of sensory-neural system with involvement of several dozen genes. Whole-exome sequencing (WES) is capable of discovering known and novel genes involved with HL. MATERIALS AND METHODS: Two pedigrees with HL background from K...

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Detalles Bibliográficos
Autores principales: Pourreza, Mohammad Reza, Mohammadi, Hannane, Sadeghian, Ladan, Asgharzadeh, Samira, Sehhati, Mohammadreza, Tabatabaiefar, Mohammad Amin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233028/
https://www.ncbi.nlm.nih.gov/pubmed/30505812
http://dx.doi.org/10.4103/abr.abr_80_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233028/
https://www.ncbi.nlm.nih.gov/pubmed/30505812
http://dx.doi.org/10.4103/abr.abr_80_18

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