Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

BACKGROUND: Hearing loss is the most common sensory defect, and it affects over 6% of the population worldwide. Approximately 50–60% of hearing loss patients are attributed to genetic causes. Currently, more than 100 genes have been reported to cause non-syndromic hearing loss. It is possible and ef...

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Detalles Bibliográficos
Autores principales: Zhou, Yingjie, Tariq, Muhammad, He, Sijie, Abdullah, Uzma, Zhang, Jianguo, Baig, Shahid Mahmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368710/
https://www.ncbi.nlm.nih.gov/pubmed/32682410
http://dx.doi.org/10.1186/s12881-020-01087-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368710/
https://www.ncbi.nlm.nih.gov/pubmed/32682410
http://dx.doi.org/10.1186/s12881-020-01087-x

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