Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort

BACKGROUND: Hearing loss or hearing impairment is a clinically and genetically heterogeneous disorder. More than 117 genes were discovered to date in hereditary, nonsyndromic hearing loss (NSHL). Identifying novel gene variants and their frequency in specific populations is valuable for public healt...

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Detalles Bibliográficos
Autores principales: Khan, Amjad, Han, Shirui, Wang, Rongrong, Ansar, Muhammad, Ahmad, Wasim, Zhang, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732339/
https://www.ncbi.nlm.nih.gov/pubmed/31389194
http://dx.doi.org/10.1002/mgg3.917

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732339/
https://www.ncbi.nlm.nih.gov/pubmed/31389194
http://dx.doi.org/10.1002/mgg3.917

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