A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population

BACKGROUND: Congenital deafness is one of the most distressing disorders affecting humanity and exhibits a high incidence worldwide. Most cases of congenital deafness in the Chinese population are caused by defects in a limited number of genes. A convenient and reliable method for detecting common d...

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Detalles Bibliográficos
Autores principales: Li, Siping, Peng, Qi, Liao, Shengyun, Li, Wenrui, Ma, Qiang, Lu, Xiaomei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432070/
https://www.ncbi.nlm.nih.gov/pubmed/28505178
http://dx.doi.org/10.1371/journal.pone.0177196

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432070/
https://www.ncbi.nlm.nih.gov/pubmed/28505178
http://dx.doi.org/10.1371/journal.pone.0177196

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