Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing

Hearing loss is a common neurosensory disorder, approximately half of the cases are caused by genetic factors, and approximately 70% of hereditary hearing impairments are nonsyndromic hearing loss (NSHL). The mutations of GJB2 (gap junction beta-2 protein), GJB3 (gap junction beta-3 protein), SLC26A...

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Detalles Bibliográficos
Autores principales: Zhao, Pingsen, Lin, Lifang, Lan, Liubing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160144/
https://www.ncbi.nlm.nih.gov/pubmed/30235673
http://dx.doi.org/10.1097/MD.0000000000012285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160144/
https://www.ncbi.nlm.nih.gov/pubmed/30235673
http://dx.doi.org/10.1097/MD.0000000000012285

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